Examining FDA's Medical Device User Fee Program :  hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth Congress, first session, March 28, 2017. 
 Examining Food and Drug Administration's Medical Device User Fee Program 

 - 1 online resource (iii, 107 pages) :  illustrations 
<br/><br/> "Serial No. 115-20."  CRDP Program record. 
<br/><br/>Includes bibliographical references. 
<br/><br/><label>Subjects--Corporate Names: </label><br/>United States. Food and Drug Administration --Rules and practice.
<br/><br/><label>Subjects--Topical Terms: </label><br/>User charges--Law and legislation--United States.<br/>Medical instruments and apparatus industry--Law and legislation--United States.
<br/><br/><label>Index Terms--Genre/Form: </label><br/>Legislative hearings.
<br/><br/><label>LC Class. No.: </label>KF27  / .E553 2017j 
<br/><br/><label>GPO Item No.: </label>1019-C-01 (online) 
<br/><br/><label>Gov. Doc. Class. No.: </label>Y 4.C 73/8:115-20 
<br/><br/><label>Report. No.: </label>Serial no. 115-20 (United States. Congress. House. Committee on Energy and Commerce)