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040 a| GPOc| GPOd| MvI;

042 a| pcc;

043 a| n-us---;

049 a| ERE#;

074 a| 0546-D (online);

086 0 a| GA 1.13:GAO-09-190;

088 a| GAO-09-190;

110 1 a| United States.b| Government Accountability Office.=| ^A580995;

245 10 a| Medical devices :b| FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees.;

246 3 a| Medical devices :b| Food and Drug Administration should take steps to ensure that high risk device types are approved through the most stringent premarket review process;

246 30 a| Food and Drug Administration should take steps to ensure that high-risk device types are approved through the most stringent premarket review process;

246 17 a| Medical device premarket review;

260 a| [Washington, D.C.] :b| U.S. Govt. Accountability Office,c| [2009];

300 a| iv, 57 p. :b| digital, PDF file;

336 a| textb| txt2| rdacontent;

337 a| computerb| c2| rdamedia;

338 a| online resourceb| cr2| rdacarrier;

538 a| Mode of access: Internet from GAO web site. Address as of 2/17/09: http://www.gao.gov/new.items/d09190.pdf; current access available via PURL.;

500 a| Title from title screen (viewed Feb. 17, 2009).;

500 a| "January 2009.";

504 a| Includes bibliographical references.;

500 a| "GAO-09-190.";

500 a| GPO Cataloging Record Distribution Program (CRDP).;

610 10 a| United States.b| Food and Drug Administrationx| Management.=| ^A1253;

650 0 a| Medical instruments and apparatusx| Standardsz| United States.=| ^A1043489;

610 12 a| United States.b| Food and Drug Administration.=| ^A1253;

776 0 a| United States. Government Accountability Office.t| Medical devices : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review processh| iv, 57 p.w| (OCoLC)300161424;

856 40 u| https://purl.fdlp.gov/GPO/LPS109040;

949 a| Click on web addressw| asish| joyner94;

596 a| 1;

998 a| 1483643;

999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| MQ2858827l| JNETm| JOYNERr| Ys| Yt| JNE1DOu| 3/23/2009x| EDOCUMENTz| JERESOURCEo| .STAFF. 0;

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

Author/creator	United States
Format	Electronic
Publication Info	[Washington, D.C.] : U.S. Govt. Accountability Office, [2009]
Description	iv, 57 p. : digital, PDF file
Supplemental Content	https://purl.fdlp.gov/GPO/LPS109040
Subjects	United States. Food and Drug Administration--Management. United States. Food and Drug Administration. Medical instruments and apparatus--Standards. --United States. Equipment and Supplies--standards. --United States. --Statistics.

Variant 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
Portion of title	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
General note	Title from title screen (viewed Feb. 17, 2009).
General note	"January 2009."
General note	"GAO-09-190."
General note	GPO Cataloging Record Distribution Program (CRDP).
Bibliography note	Includes bibliographical references.
Technical details	Mode of access: Internet from GAO web site. Address as of 2/17/09: http://www.gao.gov/new.items/d09190.pdf; current access available via PURL.
Issued in other form	United States. Government Accountability 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.
Technical rpt number	GAO-09-190
GPO item number	0546-D (online)
Govt. docs number	GA 1.13:GAO-09-190

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

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