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Electronic Book

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.

Connect to
Connect to https://www.govinfo.gov/content/pkg/CHRG-109hhrg30528/pdf/CHRG-109hhrg30528.pdf

Copies

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
	9780160777813
Gpo Item No.	1016-A (online)
Sudoc No.	Y 4.G 74/7:M 46/30