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  E-mail Message: I thought you might be interested in this item at http://www.worldcat.org/oclc/79832529 Title: 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. Publisher: Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2006. ISBN/ISSN: 016077781X 9780160777813 OCLC:79832529

  
  

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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.

Author:	United States. Congress. House. Committee on Government Reform.
Publisher:	Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2006.
Edition/Format:	Book : National government publication : EnglishView all editions and formats
Rating:	(not yet rated) 0 with reviews - Be the first.
Subjects	Disposable medical devices -- Reuse -- Government policy -- United States. Medical instruments and apparatus -- Safety regulations -- United States.
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