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Showing 1 - 20 results of 65 for search '"Medical instruments and apparatus Safety regulations United States"', query time: 0.21s Refine Results
  1. 1
    Medical devices : hearings before the Subcommittee on Public Health and Environment of the Committee on Interstate and Foreign Commerce, House of Representatives, Ninety-third Congress, first session on H.R. 6073 and H.R. 9984, bills to protect the public health by amending the Federal Food, Drug, and Cosmetic Act to assure the safety and effectiveness of medical devices : H.R. 539, a bill to create a national commission to study quality controls and manufacturing procedures of medical devices, surgical instruments, artificial organs and limbs, therapeutic instruments and devices, and other medical and hospital equipment, and for other purposes : H.R. 10061, a bill to regulate defective, ineffective, and unreliable medical devices, October 23 and 24, 1973.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  2. 2
    Medical device amendments, 1973 : hearings before the Subcommittee on Health of the Committee on Labor and Public Welfare, United States Senate, Ninety-third Congress, first session on S. 2368, to protect the public health by amending the Federal Food, Drug, and Cosmetic Act to assure the safety and effectiveness of medical devices : S. 1446, to protect the public health by amending the Federal, Food, Drug, and Cosmetic Act to assure the safety and effectiveness of medical devices : S. 1337, to protect the public health by amending the Federal Food, Drug, and Cosmetic Act to assure the safety, reliability, and effectiveness of medical devices, September 14 and 17, 1973.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  3. 3
    Medical devices reporter (CCH).
    by CCH Incorporated
    Published 2010
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
    Coverage: current publication
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  4. 4
    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, a bill to amend the Federal Food, Drug, and Cosmetic Act to provide for the safety and effectiveness of medical devices intended for human use : H.R. 974, a bill to regulate defective, ineffective, and unreliable medical devices and S. 510, a bill to protect the public health by amending the Federal Food, Drug, and Cosmetic Act to assure the safety and effectiveness of medical devices, July 28, 29, 30, and 31, 1975.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  5. 5
    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, a bill to amend the Federal Food, Drug, and Cosmetic Act to make improvements in the regulation of medical devices, and for other purposes, November 6, 1989 and July 17, 1990.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  6. 6
    Medical device legislation introduced in the 93d Congress /
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  7. 7
    Medical device legislation--1975 /
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  8. 8
    Suggested amendments to H.R. 9984 (relating to medical devices) and comparison of House and Senate bills /
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  9. 9
    Medical device amendments, 1973. Hearings, Ninety-third Congress, first session, on S. 2368 ...
    Subjects: “...Medical instruments and apparatus Safety regulations United States...”
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  10. 10
    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
    Subjects: “...Medical instruments and apparatus Safety regulations United States...”
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  11. 11
    Medical devices. Hearings, Ninety-third Congress, first session ...
    Subjects: “...Medical instruments and apparatus Safety regulations United States...”
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  12. 12
    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.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  13. 13
    Reprocessing of single-use medical devices : hearing of the Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Sixth Congress, second session on examining the safety and effectiveness of certain medical devices, focusing on the practice of reprocessing and reusing certain medical devices that were designed, manufactured, and approved by FDA for use in a single patient, during a single procedure, June 27, 2000.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  14. 14
    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
    Subjects: “...Medical instruments and apparatus Safety regulations United States...”
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  15. 15
    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.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  16. 16
    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
    Subjects: “...Medical instruments and apparatus Safety regulations United States...”
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  17. 17
    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.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  18. 18
    FDA oversight : medical devices : hearing before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, House of Representatives, Ninety-seventh Congress, second session, July 16, 1982.
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
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  19. 19
    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
    Subjects: “...Medical instruments and apparatus Safety regulations United States...”
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  20. 20
    Reinventing regulation of drugs and medical devices /
    Subjects: “...Medical instruments and apparatus Safety regulations United States....”
    HeinOnline Reports of U.S. Presidential Commissions
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