01438nam 2200409 a 450 991069792930332120090226162514.0(CKB)5470000002393702(OCoLC)310982445(EXLCZ)99547000000239370220090226d2009 ua 0engurmn|||||||||txtrdacontentcrdamediacrrdacarrierMedical 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[Washington, D.C.] :U.S. Govt. Accountability Office,[2009]iv, 57 pages digital, PDF fileTitle from title screen (viewed Feb. 17, 2009)."January 2009.""GAO-09-190."Includes bibliographical references.Medical devices Medical instruments and apparatusStandardsUnited StatesEquipment and SuppliesstandardsUnited StatesStatistics.Statistics.lcgftMedical instruments and apparatusStandardsEquipment and Suppliesstandards.GPOGPOBOOK9910697929303321Medical devices2002516UNINA