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

Description
Item Description:	Title from title screen (viewed Feb. 17, 2009). "January 2009." "GAO-09-190." Electronic resource.
Physical Description:	iv, 57 pages : digital, PDF file.
Format:	Mode of access: Internet from GAO web site. Address as of 2/17/09: http://www.gao.gov/new.items/d09190.pdf ; current access available via PURL.
Bibliography:	Includes bibliographical references.