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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

Corporate Author:
United States. Government Accountability Office
Additional Titles:
Medical devices : Food and Drug Administration should take steps to ensure that high risk device types are approved through the most stringent premarket review process, Food and Drug Administration should take steps to ensure that high-risk device types are approved through the most stringent premarket review process, and Medical device premarket review
Published:
[Washington, D.C.] : U.S. Govt. Accountability Office, [2009]
Physical Description:
iv, 57 pages : digital, PDF file
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Restrictions on Access:
Free-to-read Unrestricted online access
Report Numbers:
GA 1.13:GAO-09-190
GAO-09-190
Subject(s):
Note:
Title from title screen (viewed Feb. 17, 2009).
"January 2009."
"GAO-09-190."
Bibliography Note:
Includes bibliographical references.
Technical Details:
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.
View MARC record | catkey: 5098268