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100   $a20181207d2018      ua             0
101 0 $aeng
135   $aurbn||||a||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 10$aExamining FDA's Medical Device User Fee Program $ehearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth Congress, first session, March 28, 2017
210  1$aWashington :$cU.S. Government Publishing Office,$d2018.
215   $a1 online resource (iii, 107 pages) $cillustrations
300   $a"Serial No. 115-20."
320   $aIncludes bibliographical references.
517   $aExamining FDA's Medical Device User Fee Program 
606   $aUser charges$xLaw and legislation$zUnited States
606   $aMedical instruments and apparatus industry$xLaw and legislation$zUnited States
608   $aLegislative hearings.$2lcgft
615  0$aUser charges$xLaw and legislation
615  0$aMedical instruments and apparatus industry$xLaw and legislation
801  0$bGPO
801  1$bGPO
801  2$bGPO
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801  2$bOCLCF
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801  2$bOCLCO
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801  2$bOCLCQ
801  2$bGPO
906   $aBOOK
912   $a9910711658403321
996   $aExamining FDA's Medical Device User Fee Program$93463765
997   $aUNINA