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100   $a20090226d2009      ua             0
101 0 $aeng
135   $aurmn|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 10$aMedical devices$b[electronic resource] $eFDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees
210  1$a[Washington, D.C.] :$cU.S. Govt. Accountability Office,$d[2009]
215   $aiv, 57 pages $cdigital, PDF file
300   $aTitle from title screen (viewed Feb. 17, 2009).
300   $a"January 2009."
300   $a"GAO-09-190."
320   $aIncludes bibliographical references.
517   $aMedical devices 
606   $aMedical instruments and apparatus$xStandards$zUnited States
606   $aEquipment and Supplies$xstandards
607   $aUnited States
608   $aStatistics.
608   $aStatistics.$2lcgft
615  0$aMedical instruments and apparatus$xStandards
615 12$aEquipment and Supplies$xstandards.
801  0$bGPO
801  1$bGPO
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912   $a9910697929303321
996   $aMedical devices$92002516
997   $aUNINA