Catalog Record: Medical device safety : how FDA regulates the reprocessing of supposedly single-use devices : hearing before the Committee on Government Reform, House of Representatives, One Hundred Ninth Congress, second session, September 26, 2006 | HathiTrust Digital Library

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Medical device safety :
how FDA regulates the reprocessing of supposedly single-use devices : hearing before the Committee on Government Reform, House of Representatives, One Hundred Ninth Congress, second session, September 26, 2006.

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Corporate Author: United States.
Language(s): English
Published: Washington : U.S. G.P.O. : 2006.
Subjects: Medical instruments and apparatus > Medical instruments and apparatus / Safety regulations > Medical instruments and apparatus / Safety regulations / United States.
Disposable medical devices > Disposable medical devices / Reuse > Disposable medical devices / Reuse / Government policy > Disposable medical devices / Reuse / Government policy / United States.
Note: "Serial no. 109-190."
Shipping list no.: 2007-0127-P.
Distributed to some depository libraries in microfiche.
Also available via Internet from the GPO Access web site. Address as of 1/24/07: http://frwebgate.access.gpo.gov/cgi-bin/getdoc.cgi?dbname=109%5F house%5Fhearings&docid=f:30528.pdf; current access available via PURL.
Physical Description: iii, 99 p. ; 24 cm.
ISBN: 9780160777813
016077781X
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