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ElectronicResource GovDoc

Corporate Author

United States. Government Accountability Office.

Title Medical devices [electronic resource] : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees.

Imprint

[Washington, D.C.] : U.S. Govt. Accountability Office, [2009]

Connect to
Connect to https://permanent.fdlp.gov/LPS109040/LPS109040/www.gao.gov/new.items/d09190.pdf

Copies

Location	Call No.	OPAC Message	Status
Axe Federal Documents Online	GA 1.13:GAO-09-190	---	Available

Description	iv, 57 p. : digital, PDF file
System Details	Mode of access: Internet from GAO web site.
Note	Title from title screen (viewed Feb. 17, 2009).
	"January 2009."
Bibliography	Includes bibliographical references.
Note	"GAO-09-190."
Subject	United States. Food and Drug Administration -- Management.
	Medical instruments and apparatus -- Standards -- United States.
	United States. Food and Drug Administration.
	Equipment and Supplies -- standards -- United States -- Statistics.
Added Title	Medical devices : Food and Drug Administration should take steps to ensure that high risk device types are approved through the most stringent premarket review process
	Food and Drug Administration should take steps to ensure that high-risk device types are approved through the most stringent premarket review process
Running Title	Medical device premarket review
Other Form:	United States. Government Acountability Office. Medical devices : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process iv, 57 p. (OCoLC)300161424
Gpo Item No.	0546-D (online)
Sudoc No.	GA 1.13:GAO-09-190