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Corporate Author United States. Congress. House. Committee on Government Reform.

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.

Imprint Washington : U.S. G.P.O. : For sale by the Supt. of Docs., U.S. G.P.O., 2006.


Location Call No. OPAC Message Status
 Axe Federal Documents Online  Y 4.G 74/7:M 46/30    ---  Available
Description iii, 99 p. ; 24 cm.
Note Distributed to some depository libraries in microfiche.
Form Mode of access via the GPO Access web site.
Bibliography Includes bibliographical references.
Note "Serial no. 109-190."
Subject Disposable medical devices -- Reuse -- Government policy -- United States.
Medical instruments and apparatus -- Safety regulations -- United States.
ISBN 016077781X
Gpo Item No. 1016-A (online)
Sudoc No. Y 4.G 74/7:M 46/30

Available items only