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.
|Corporate Author:||United States.|
Washington : U.S. G.P.O. : 2006.
Disposable medical devices
> Government policy
> United States.
Medical instruments and apparatus > Safety regulations > United States.
Distributed to some depository libraries in microfiche.
Shipping list no.: 2007-0127-P.
"Serial no. 109-190."
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%5Fhouse%5Fhearings&docid=f:30528.pdf; current access available via PURL.
iii, 99 p. ;
|Original Classification Number:||Y 4.G 74/7:M 46/30|
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- Full view4.G 74/7:M 46/30 (original from Penn State University)