Showing 121 - 140 results of 201 for search 'Center for Devices and Radiological Health (U.S.)', query time: 0.06s Refine Results
  1. 121

    Guidance for submission of information on medical ultraviolet lamps pursuant to 21 CFR 1002.10 and 1002.12

    Rockville, Md. : U.S. Dept. of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1985
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
    Format: Government Document Book


  2. 122

    Medical device listing information and instructions

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
    Format: Government Document Book


  3. 123

    Classification names for medical devices and in vitro diagnostic products

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1991
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
    Format: Government Document Book


  4. 124

    Emerging electromagnetic medicine

    New York : Springer-Verlag, 1990
    Format: Book


  5. 125

    Quality control guide for sunlamp products.

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
    Format: Government Document Book


  6. 126

    Guide for the filing of annual reports for x-ray components and systems

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1985
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
    Format: Government Document Book


  7. 127

    Import and export regulatory requirements for medical devices

    Rockville, Md. : Washington, D.C. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; For sale by the Supt. of Docs., U.S. G.P.O., 1988
    “…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
    Format: Government Document Book


  8. 128

    Medical device GMP guidance for FDA investigators

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administrationn, Center for Devices and Radiological Health, 1984
    “…Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance…”
    Format: Government Document Book


  9. 129

    Annual report

    “…Center for Devices and Radiological Health (U.S.). Office of Device Evaluation…”
    Format: Government Document Serial


  10. 130

    Device recalls : a study of quality problems

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1990
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance and Surveillance…”
    Format: Government Document Book


  11. 131

    Medical devices standards activities report

    “…Center for Devices and Radiological Health (U.S.). Office of Standards and Regulations…”
    Format: Government Document Serial


  12. 132

    Guideline for the manufacture of in vitro diagnostic products.

    Rockville, Md. : Division of Compliance Programs, Office of Compliance and Surveillance, Center for Devices and Radiological Health, Food and Drug Administration, 1990
    “…Center for Devices and Radiological Health (U.S.). Division of Compliance Programs…”
    Format: Government Document Book


  13. 133

    The regulation of AIDS-related medical devices by Rivera, Richard J.

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1991
    “…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
    Format: Government Document Book


  14. 134

    Premarket notification--510(k) : regulatory requirements for medical devices

    Rockville, Md. : Washington, D.C. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; For sale by the Supt. of Docs., U.S. G.P.O., 1988
    “…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
    Format: Government Document Book


  15. 135

    Medical devices standards activities report

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1989
    “…Center for Devices and Radiological Health (U.S.). Office of Standards and Regulations…”
    Format: Government Document Book


  16. 136

    Clarification of radiation control regulations for diagnostic x-ray equipment

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1989
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance and Surveillance…”
    Format: Government Document Book


  17. 137

    Preproduction quality assurance planning : recommendations for medical device manufacturers

    Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1989
    “…Center for Devices and Radiological Health (U.S.). Office of Compliance and Surveillance…”
    Format: Government Document Book


  18. 138

    Center for Devices and Radiological Health publications index

    Rockville, Md. : The Center, 1988
    “…Center for Devices and Radiological Health (U.S.). Publications Support Branch…”
    Format: Government Document Serial


  19. 139

    Premarket approval (PMA) manual

    Rockville, Md. : [Washington, D.C.] : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; [Supt. of Docs., U.S. G.P.O., distributor], 1986
    “…Center for Devices and Radiological Health (U.S.). Office of Device Evaluation…”
    Format: Government Document Book


  20. 140

    Device good manufacturing practices manual

    Rockville, Md. : Washington, D.C. : The Office ; For sale by the Supt. of Docs., U.S. G.P.O., 1984
    3d ed.
    “…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
    Format: Government Document Book