Search results for: Center for Devices and Radiological Health (U.S.). Office of Compliance

Showing 1 - 13 results of 13 Refine Results
  1. 1

    Medical device listing information and instructions

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984
    Physical Description: 43 pages : forms ; 28 cm.
    Government Document Book
  2. 2

    Quality control guide for sunlamp products

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1988
    Physical Description: vi, 30 pages : illustrations ; 28 cm.
    Government Document Book
  3. 3

    Classification names for medical devices and in vitro diagnostic products

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1991
    Physical Description: 265 pages ; 28 cm.
    Government Document Book
  4. 4

    Classification names for medical devices

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984
    Physical Description: 70 pages ; 28 cm.
    Government Document Book
  5. 5

    Classification names for in vitro diagnostic products

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984
    Physical Description: 48 pages ; 28 cm.
    Government Document Book
  6. 6

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

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1985
    Physical Description: i, 5 pages : 1 illustration, forms ; 28 cm
    Government Document Book
  7. 7

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

    Published: U.S. Department of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1985
    Physical Description: 24 pages : forms ; 28 cm
    Government Document Book
  8. 8

    Guide for submission of information on industrial x-ray equipment required pursuant to 21 CFR 1002.10

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1985
    Physical Description: 9 pages ; 28 cm
    Government Document Book
  9. 9

    Guidance for industry and for FDA staff : enforcement priorities for single-use devices reprocessed by third parties and hospitals.

    Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Division of Enforcement, Office of Compliance, 2000
    Connect to online resource - All users (Federal Depository Library Program Persistant URL)
    Government Document Electronic eBook
  10. 10

    Guidance for industry and for FDA staff : enforcement priorities for single-use devices reprocessed by third parties and hospitals.

    Published: U.S. Department of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Division of Enforcement, Office of Compliance, 2000
    Government Document Microfilm Book
  11. 11

    Draft guidance for industry and FDA : consumer-directed broadcast advertising of restricted devices.

    Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Office of Compliance, 2004
    Physical Description: 1 online resource (5 pages)
    Connect to online resource - All users (Federal Depository Library Program Persistant URL)
    Government Document Electronic eBook
  12. 12

    Device recalls : a study of quality problems

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1990
    Physical Description: vi, 16 pages : illustrations ; 28 cm.
    Government Document Book
  13. 13

    Preproduction quality assurance planning : recommendations for medical device manufacturers

    Published: U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1989
    Physical Description: vi, 18 pages ; 28 cm.
    Government Document Book