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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.
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.
United States.
U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O.,
2006.
{{indexedTitle}} appears in the content of this record.
{{title}} can only be used in the library.
A copy of {{title}} has been set aside for library use only.
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.
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.
United States.
U.S. Government Printing Office,
2006.