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

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

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Bibliographic Details
Corporate Author: United States. Department of Health and Human Services. Office of Inspector General (Author)
Format: Government Document Online Book
Language:English
Published: 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:http://purl.fdlp.gov/GPO/gpo71036
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Description
Physical Description:1 online resource (27 pages) : illustrations

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