Search results for: Center for Devices and Radiological Health (U.S.). Office of Compliance
Showing 1 - 13 results of 13
Refine Results
-
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, 1984Physical Description: 43 pages : forms ; 28 cm.Holdings: Loading…
Government Document Book Loading… -
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, 1988Physical Description: vi, 30 pages : illustrations ; 28 cm.Holdings: Loading…
Government Document Book Loading… -
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, 1991Physical Description: 265 pages ; 28 cm.Holdings: Loading…
Government Document Book Loading… -
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, 1984Physical Description: 70 pages ; 28 cm.Holdings: Loading…
Government Document Book Loading… -
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, 1984Physical Description: 48 pages ; 28 cm.Holdings: Loading…
Government Document Book Loading… -
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, 1985Physical Description: i, 5 pages : 1 illustration, forms ; 28 cmHoldings: Loading…
Government Document Book Loading… -
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, 1985Physical Description: 24 pages : forms ; 28 cmHoldings: Loading…
Government Document Book Loading… -
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, 1985Physical Description: 9 pages ; 28 cmHoldings: Loading…
Government Document Book Loading… -
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, 2000Holdings: Loading…Connect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
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, 2000Holdings: Loading…
Government Document Microfilm Book Loading… -
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, 2004Physical Description: 1 online resource (5 pages)Holdings: Loading…Connect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
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, 1990Physical Description: vi, 16 pages : illustrations ; 28 cm.Holdings: Loading…
Government Document Book Loading… -
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, 1989Physical Description: vi, 18 pages ; 28 cm.Holdings: Loading…
Government Document Book Loading…