Medical devices : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees.

Bibliographic Details
Corporate Author:	United States. Government Accountability Office
Format:	Government Document eBook
Language:	English
Published:	[Washington, D.C.] : U.S. Govt. Accountability Office, [2009]
Subjects:	United States. > Food and Drug Administration > Management. United States. > Food and Drug Administration. Medical instruments and apparatus > Standards > United States. Equipment and Supplies > standards > United States > Statistics.
Online Access:	https://purl.fdlp.gov/GPO/LPS109040

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