Center for Devices and Radiological Health (U.S.)

Identifiers

Open LibraryOL4546305A

Top Subjects

United States (10)
Medical instruments and apparatus (7)
Equipment and Supplies (3)
Standards (3)
Handbooks, manuals (2)
Radiography (2)
Tables (2)

Books by Center for Devices and Radiological Health (U.S.)

Total count: 21

Extremity radiography following traumaan overview

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1984-01-01
An Overview of the medical device reporting regulationfinal rule, effective December 13, 1984, 21 CFR part 803

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1984-01-01
Vignettes of early radiation workerstranscripts of the videotape series

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1984-01-01
Device good manufacturing practices manual3rd ed.

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1984-01-01
Evaluation of radiation exposure from diagnostic radiology examinationsgeneral recommendations

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1985-01-01
The Selection of patients for x-ray examinationsskull x-ray examination for trauma

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1986-01-01
Laser light show safetywho's responsible?Rev. May 1986.

U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1986-01-01
Guideline on general principles of process validation

U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration1987-01-01
In vitro diagnostic devicesguidance for the preparation of 510(k) submissions

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1987-01-01
Medical device establishment registrationinformation and instructions

U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1987-01-01
Everything you always wanted to know about the medical device amendments ... and weren't afraid to ask2nd ed.

U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1988-01-01
Applications of DNA probes for the diagnosis of human infectious diseasesan overview

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1988-01-01
Handbook of selected tissue doses for projections common in diagnostic radiology

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1988-01-01
Yorickthe CDRH bionic skeleton

U.S. Department of Health and Human Services, Public Health Service, Food and Drug Administration1989-01-01
A follow-up study of persons who had iodine-131 and other diagnostic procedures during childhood and adolescence

U.S. Dept. of Health and Human Sevices, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1989-01-01
Handbook of selected tissue doses for the upper gastrointestinal fluoroscopic examination

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1992-01-01
Import of medical devicesa workshop manual

U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health1993-01-01
FDA's Center for Devices and Radiological Healtha profile

The Center1995-01-01
Enforcement priorities for single-use devices reprocessed by third parties and hospitalsguidance for industry and for FDA staff

The Department, Food and Drug Administration, Center for Devices and Radiological Health2000-01-01
FDA and industry actions on premarket approval applications (PMAs), effect on FDA review clock and goals

U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health2008-01-01
Guidance for industry, FDA staff, and FDA-accredited third partiesManufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA)

U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health2009-01-01