LEADER 01620nam  2200409   450 
001 9910707492403321
005 20160810093851.0
035   $a(CKB)5470000002464600
035   $a(OCoLC)956437209
035   $a(OCoLC)995470000002464600
035   $a(EXLCZ)995470000002464600
100   $a20160810d2013      ua             0
101 0 $aeng
135   $aurmn|||||||||
181   $2rdacontent
182   $2rdamedia
183   $2rdacarrier
200 10$aFDA's clearance of medical devices through the 510(k) process
210  1$a[Washington, D.C.] :$cDepartment of Health and Human Services, Office of Inspector General,$d2013.
215   $a1 online resource (27 pages) $cillustrations
300   $aTitle from title screen (viewed Aug. 8, 2016).
300   $a"September 2013."
300   $a"OEI-04-10-00480."
320   $aIncludes bibliographical references.
517   $aFDA's clearance of medical devices through the 510
606   $aMedical instruments and apparatus$xGovernment policy$zUnited States
606   $aMedical instruments and apparatus$zUnited States$vClassification
606   $aMedical instruments and apparatus$xTechnological innovations$xGovernment policy$zUnited States
615  0$aMedical instruments and apparatus$xGovernment policy
615  0$aMedical instruments and apparatus
615  0$aMedical instruments and apparatus$xTechnological innovations$xGovernment policy
801  0$bGPO
801  1$bGPO
906   $aBOOK
912   $a9910707492403321
996   $aFDA's clearance of medical devices through the 510(k) process$93299498
997   $aUNINA