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LEADER 01968nam a2200469 i 4500

001 ocn956437209;

003 OCoLC;

005 20161027130420.0;

006 m o d f ;

007 cr mn|||||||||;

008 160810s2013 dcua ob f000 0 eng c;

035 a| (Sirsi) o956437209;

042 a| pcc;

043 a| n-us---;

049 a| ERE#;

074 a| 0445-B-07 (online);

086 0 a| HE 1.75:OEI-04-10-00480;

088 a| OEI-04-10-00480;

245 10 a| FDA's clearance of medical devices through the 510(k) process.;

246 3 a| Food and Drug Administration's clearance of medical devices through the 510(k) process;

246 1 i| Running title:a| FDA's clearance of medical devices through the 510(k) process;

264 1 a| [Washington, D.C.] :b| Department of Health and Human Services, Office of Inspector General,c| 2013.;

300 a| 1 online resource (27 pages) :b| illustrations;

336 a| text2| rdacontent;

337 a| computer2| rdamedia;

338 a| online resource2| rdacarrier;

500 a| Title from title screen (viewed Aug. 8, 2016).;

500 a| "September 2013.";

500 a| "OEI-04-10-00480.";

500 a| CRDP Project record.;

504 a| Includes bibliographical references.;

650 0 a| Medical instruments and apparatusx| Government policyz| United States.=| ^A3247;

650 0 a| Medical instruments and apparatusz| United Statesv| Classification.=| ^A3247;

856 40 u| https://purl.fdlp.gov/GPO/gpo71036;

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

998 a| 4535419;

998 a| u4535419;

596 a| 1;

999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| 4535419-1001l| JNETm| JOYNERr| Ys| Yt| JNE1DOu| 9/9/2016x| EDOCUMENTz| JERESOURCE;

FDA's clearance of medical devices through the 510(k) process.

Author/creator	United States
Format	Electronic
Publication	[Washington, D.C.] : Department of Health and Human Services, Office of Inspector General, 2013.
Description	1 online resource (27 pages) : illustrations
Supplemental Content	https://purl.fdlp.gov/GPO/gpo71036
Subjects	Medical instruments and apparatus--Government policy. --United States. Medical instruments and apparatus--United States. --Classification. Medical instruments and apparatus--Technological innovations. --Government policy. --United States.

Variant title	Food and Drug Administration's clearance of medical devices through the 510(k) process
Variant title	Running title: FDA's clearance of medical devices through the 510(k) process
General note	Title from title screen (viewed Aug. 8, 2016).
General note	"September 2013."
General note	"OEI-04-10-00480."
General note	CRDP Project record.
Bibliography note	Includes bibliographical references.
Technical rpt number	OEI-04-10-00480
GPO item number	0445-B-07 (online)
Govt. docs number	HE 1.75:OEI-04-10-00480

Library	Location	Call Number	Status	Item Actions
	Electronic Resources	Access Content Online	✔ Available

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