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Medical instruments and apparatus -- Safety regulations -- United States

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• Medical instruments and apparatus -- Safety regulations
• Medical instruments and apparatus -- Law and legislation -- United States
• Medical instruments and apparatus -- United States
• Safety regulations -- United States

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• Medical instruments and apparatus -- Safety regulations -- United States -- Periodicals
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• Federal Policies and the Medical Devices Industry (1984), by United States Congress Office of Technology Assessment (PDF files at Princeton)
• Preamble compilation : Medical devices, March 1936-March 1978. (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration ;, 1981), by United States Food and Drug Administration (page images at HathiTrust)
• Federal policies and the medical devices industry. (Congress of the U.S., Office of Technology Assessment, 1984), by United States Congress Office of Technology Assessment (page images at HathiTrust)
• Medical devices : FDA's implementation of the medical device reporting regulation : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives (The Office, 1989), by United States General Accounting Office and United States. Congress. Committee on Energy and Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Reinventing drug & medical device regulations (National Performance Review, 1995), by Bill Clinton, Al Gore, and National Performance Review (U.S.) (page images at HathiTrust)
• Premarket notification, 510(k) : regulatory requirements for medical devices (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; Washington, D.C. : For sale by the Supt. of Docs., U.S. G.P.O., 1990), by Center for Devices and Radiological Health (U.S.). Office of Training and Assistance (page images at HathiTrust)
• Medical device legislation introduced in the 93d Congress (U.S. Govt. Print. Off., 1973), by United States. Congress. House. Committee on Interstate and Foreign Commerce. Subcommittee on Public Health and Environment (page images at HathiTrust)
• Medical devices hearings, Ninety-third Congress, first session .. (U.S. Govt. Print. Off., 1974), by United States. Congress. House. Committee on Interstate and Foreign Commerce. Subcommittee on Public Health and Environment (page images at HathiTrust)
• Medical device amendments, 1973 hearings, Ninety-third Congress, first session, on S. 2368 .. (U.S. Govt. Print. Off., 1974), by United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health (page images at HathiTrust)
• Medical device amendments of 1975 hearings before the Subcommittee on Health and the Environment of the Committee on Interstate and Foreign Commerce, House of Representatives, Ninety-fourth Congress, first session, on H.R. 5545 ... H.R. 974 ... S. 510 .... (U.S. Govt. Print. Off., 1975), by United States. Congress. House. Committee on Interstate and Foreign Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Medical device legislation, 1975 (U.S. Govt. Print. Off., 1975), by United States. Congress. House. Committee on Interstate and Foreign Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• FDA and the medical device industry : hearings before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, March 25 and June 3, 1992. (U.S. G.P.O. :, 1992), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations (page images at HathiTrust)
• FDA's drug and device review process : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, February 6, 1992. (U.S. G.P.O. :, 1992), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations (page images at HathiTrust)
• Medical device safety : hearings before the Subcommittee on Health and the Environment of the Committee on Energy and Commerce, House of Representatives, One Hundred First Congress on H.R. 3095 ... November 6, 1989 and July 17, 1990. (U.S. G.P.O. :, 1990), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Medical devices : hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred First Congress, second session : on examing proposed legislation ... July 25, 1990. (U.S. G.P.O. :, 1990), by United States Senate Committee on Labor and Human Resources (page images at HathiTrust)
• Revitalizing new product development from clinical trials through FDA review : hearing of the Committee on Labor and Human Resources, United States Senate, One Hundred Fourth Congress, second session, on S. 1477 ... February 21, 1996. (U.S. G.P.O. :, 1996), by United States Senate Committee on Labor and Human Resources (page images at HathiTrust)
• FDA and the medical device industry : hearings before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, March 25 and June 3, 1992. (U.S. G.P.O. :, 1992), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations (page images at HathiTrust)
• Food, drug, cosmetic, and device enforcement amendments : hearing before the Subcommittee on Health and the Environment of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, first session, on H.R. 2597, a bill to amend the Federal Food, Drug, and Administration, July 17, 1991. (U.S. G.P.O. :, 1991), by United States. Congress. House. Committee on House and Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Food, Drug, Cosmetic, and Device Enforcement Authorities Act : hearing of the Committee on Labor and Human Resources, United States Senate, One Hundred Second Congress, second session, on S. 2135 ... May 19, 1992. (U.S. G.P.O. :, 1992), by United States Senate Committee on Labor and Human Resources (page images at HathiTrust)
• FDA's drug and device review process : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, One Hundred Second Congress, second session, February 6, 1992. (U.S. G.P.O. :, 1992), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations (page images at HathiTrust)
• More information for better patient care : hearing of the Committee on Labor and Human Resources, United States Senate, One Hundred Fourth Congress, second session, on S. 1477, to amend the Federal Food, Drug, and Cosmetic Act and the Public Health Service Act to improve the regulation of food, drugs, devices, and biological products, February 22, 1996. (U.S. G.P.O. :, 1996), by United States Senate Committee on Labor and Human Resources (page images at HathiTrust)
• FDA reform legislation : hearings before the Subcommittee on Health and Environment of the Committee on Commerce, House of Representatives, One Hundred Fourth Congress, second session, on H.R. 3199, 3200, and 3201, May 1 and 2, 1996. (U.S. G.P.O. :, 1996), by United States. Congress. House. Committee on Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Food and Drug enforcement standards for medical devices : joint hearing before the Subcommittee on Human Resources and Intergovernmental Relations and the Subcommittee on National Economic Growth, Natural Resources, and Regulatory Affairs of the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fourth Congress, first session, September 14, 1995. (U.S. G.P.O. :, 1997), by United States. Congress. House. Committee on Government Reform and Oversight. Subcommittee on Human Resources and Intergovernmental Relations and Natural Resources United States. Congress. House. Committee on Government Reform and Oversight. Subcommittee on National Economic Growth (page images at HathiTrust)
• Quality assurance needs stronger management emphasis and higher priority (The Office ;, 1992), by United States General Accounting Office and United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations (page images at HathiTrust)
• Medical devices : FDA's forecasts of problem reports and FTEs under H.R. 4640 : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives (The Office, 1988), by United States General Accounting Office and United States. Congress. Committee on Energy and Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Medical devices : underreporting of serious problems with a home apnea monitor : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives (The Office, 1990), by United States General Accounting Office and United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Reprocessing of single use medical devices (U.S. G.P.O. :, 2000), by United States Senate Committee on Health, Education, Labor, and Pensions (page images at HathiTrust)
• Medical device safety : how FDA regulates the reprocessing of supposedly single-use devices : hearing before the Committee on Government Reform, House of Representatives, One Hundred Ninth Congress, second session, September 26, 2006. (U.S. G.P.O. :, 2006), by United State House Committee on Government Reform (page images at HathiTrust)
• Federal state medical device legislation, 1973 (U.S. Dept. of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, Bureau of Medical Devices and Diagnostic Products :, 1975), by Lois A. Miller and United States. Bureau of Medical Devices and Diagnostic Products (page images at HathiTrust)
• Programs affecting safety and innovation in pediatric therapies : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 22, 2007. (U.S. G.P.O. :, 2008), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health (page images at HathiTrust)
• Ensuring safe medicines and medical devices for children : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Tenth Congress, first session, on examining ensuring safe medicines and medical devices for children, March 27, 2007. (U.S. G.P.O. :, 2008), by United States Senate Committee on Health, Education, Labor, and Pensions (page images at HathiTrust)
• Reinventing the regulation of cancer drugs : accelerating approval and expanding access (National Performance Review, 1996), by Bill Clinton, Albert Gore, and National Performance Review (U.S.) (page images at HathiTrust)
• Medical Device User Fee and Modernization Act of 2002 : report (to accompany H.R. 3580). (U.S. G.P.O., 2002), by United States House. Committee on Energy and Commerce (page images at HathiTrust)
• FDA regulation of medical devices, including the status of breast implants : joint hearing before the Subcommittee on Human Resources and Intergovernmental Relations and the Subcommittee on National Economic Growth, Natural Resources, and Regulatory Affairs of the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fourth Congress, first session, August 1, 1995. (U.S. G.P.O. :, 1996), by United States. Congress. House. Committee on Government Reform and Oversight. Subcommittee on Human Resources and Intergovernmental Relations and Natural Resources United States. Congress. House. Committee on Government Reform and Oversight. Subcommittee on National Economic Growth (page images at HathiTrust)
• Medical devices : hearing before the Committee on Labor and Human Resources, United States Senate, One Hundred First Congress, second session, on examining proposed legislation to revise and strengthen the Food and Drug Administration's regulation of medical devices, July 25, 1990. (U.S. G.P.O. :, 1991), by United States Senate Committee on Labor and Human Resources (page images at HathiTrust)
• Medical device recalls : an overview and analysis 1983-88 : report to the Chairman, Subcommittee on Health and the Environment, Committee on Energy and Commerce, House of Representatives (The Office, 1989), by United States General Accounting Office and United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• Discussion draft of the Food and Drug Administration Globalization Act legislation device and cosmetic safety provisions : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, second session, May 14, 2008. (U.S. G.P.O. :, 2008), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health (page images at HathiTrust)
• Medical devices : are current regulations doing enough for patients? : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh Congress, first session, June 18, 2009. (U.S. G.P.O. :, 2012), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health (page images at HathiTrust)
• The impact of medical device and drug regulation on innovation, jobs, and patients : a local perspective : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, first session, September 26, 2011. (U.S. G.P.O. :, 2012), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health (page images at HathiTrust)
• Tools for compliance for the medical device and in vitrol diagnostic product industries. (Dept. of Health, Education, and Welfare, Public health Service, Food and Drug Administration, Bureau of Medical Devices and Diagnostic Products , 1976), by United States. Bureau of Medical Devices and Diagnostic Products (page images at HathiTrust)
• Medical device legislation pending before the Interstate Commerce Committee, as of December 15, 1971, together with transmittal letter and summary of the administration bill H.R. 12316 . . . (U.S. Govt. Print. Off., 1971), by United States. Congress. House. Committee on Interstate and Foreign Commerce. Subcommittee on Public Health and Environment (page images at HathiTrust)
• Medical Device Amendments of 1992. (U.S. G.P.O. :, 1992), by United States (page images at HathiTrust)
• FDA and the reform of the medical device approval process (U.S. G.P.O. :, 2011), by United States Senate Special Committee on Aging (page images at HathiTrust)
• An Act to Amend the Federal Food, Drug, and Cosmetic Act to Make Improvements in the Regulation of Medical Devices, and for Other Purposes. (U.S. G.P.O. :, 1990), by United States (page images at HathiTrust)
• Everything you always wanted to know about the medical device amendments : and weren't afraid to ask. (Dept. of Health, Education, and Welfare, [Public Health Service], Food and Drug Administration, Bureau of Medical Devices, 1977), by United States. Bureau of Medical Devices (page images at HathiTrust)

• Investigational device exemptions manual (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1996), by Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance, Althea Barcome, Marsha Melvin, and James Park (page images at HathiTrust)

• Pocket supplement to preamble compilation (U.S. Dept. of Health and Human Services, Public Health Services, Food and Drug Administration ;, 1980), by United States Food and Drug Administration (page images at HathiTrust)

• Impact of medical device regulation on jobs and patients : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, first session, February 17, 2011. (U.S. G.P.O. :, 2011), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health (page images at HathiTrust)

Items below (if any) are from related and broader terms.

• Quality assurance systems and global markets: report (The Office ;, 1993), by United States General Accounting Office and United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health and the Environment (page images at HathiTrust)
• The impact of medical device and drug regulation on innovation, jobs, and patients : a local perspective : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, first session, September 26, 2011. (U.S. G.P.O. :, 2012), by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health (page images at HathiTrust)
• Device good manufacturing practices : a quality audit program for industry. (Dept. of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, Bureau of Medical Devices, Division of Compliance Programs, 1979), by United States. Bureau of Medical Devices. Division of Compliance Programs (page images at HathiTrust)
• Import/export : regulatory requirements for medical devices (U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, National Center for Devices and Radiological Health, 1983), by National Center for Devices and Radiological Health (U.S.). Office of Small Manufacturers Assistance (page images at HathiTrust)

More items available under broader and related terms at left.