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.

Author/creator United States
Format Book
Publication InfoWashington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2006.
Descriptioniii, 99 pages ; 24 cm
Supplemental Contenthttps://purl.fdlp.gov/GPO/LPS77877
Subjects

General noteDistributed to some depository libraries in microfiche.
General noteShipping list no.: 2007-0127-P.
General note"Serial no. 109-190."
Bibliography noteIncludes bibliographical references.
Other formsAlso 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.
ISBN016077781X
ISBN9780160777813
Technical rpt numberSerial no. 109-190 (United States. Congress. House. Committee on Government Reform)
GPO item number1016-A
GPO item number1016-A (online)
GPO item number1016-B (MF)
GPO item number1016-B (online)
Govt. docs number Y 4.G 74/7:M 46/30

Availability

Library Location Call Number Status Item Actions
Joyner Fed Docs Stacks Y 4.G 74/7:M 46/30 ✔ Available Place Hold