Premarket notification, 510(k)
An edition of Premarket notification, 510(k) (1986)
regulatory requirements for medical devices
By Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Publish Date
1990
Publisher
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.
Language
eng
Pages
52
Description: