FDA's clearance of medical devices through the 510(k) process.

Bibliographic Details
Corporate Author:	United States. Department of Health and Human Services. Office of Inspector General (Author)
Format:	Government Document eBook
Language:	English
Published:	[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2013.
Subjects:	Medical instruments and apparatus > Government policy > United States. Medical instruments and apparatus > United States > Classification. Medical instruments and apparatus > Technological innovations > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/gpo71036

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