Modifications to devices subject to premarket approval (PMA) : the PMA supplement decision-making process.

Bibliographic Details
Corporate Authors:	Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)
Format:	Government Document eBook
Language:	English
Published:	[Silver Spring, Md.] : [Rockville, Md.] : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health ; Center for Biologics Evaluation and Research, [2008]
Subjects:	Medical instruments and apparatus > Testing.
Online Access:	https://purl.fdlp.gov/GPO/LPS110580