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)
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.
Genre:	Classification.
Online Access:	Connect to online resource - All users (Federal Depository Library Program Persistant URL)
Physical Description:	1 online resource (27 pages) : illustrations
Variant Title:	Food and Drug Administration's clearance of medical devices through the 510(k) process FDA's clearance of medical devices through the 510(k) process
Format:	Government Document Electronic eBook

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