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001 9910698866803321
005 20090512145442.0
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035   $a(OCoLC)320845119
035   $a(EXLCZ)995470000002397196
100   $a20090512d2006      ua             0
101 0 $aeng
135   $auran|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aAnnual reports for approved premarket approval applications (PMA)$b[electronic resource]
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health :$cCenter for Biologics Evaluation and Research,$d[2006]
215   $a10 pages $cdigital, PDF file
300   $aTitle from PDF title page (viewed on May 12, 2009).
300   $a"Draft guidance".
300   $a"Document issued on: October 26, 2006".
517   $aAnnual reports for approved premarket approval applications 
606   $aMedical instruments and apparatus$zUnited States$xEvaluation
615  0$aMedical instruments and apparatus$xEvaluation.
712 02$aCenter for Devices and Radiological Health (U.S.)
712 02$aCenter for Biologics Evaluation and Research (U.S.)
801  0$bGPO
801  1$bGPO
906   $aBOOK
912   $a9910698866803321
996   $aAnnual reports for approved premarket approval applications (PMA)$93157555
997   $aUNINA