FDA 510(k) Applications Submitted by LAURIE PANNELLA

FDA 510(k) Number Submission Date Device Name Applicant
K122072 07/16/2012 WALLFLEXTM BILIARY RX STENT SYSTEM (UNCOVERED, PARTIALLY COVERED, AND FULLY COVERED) WALLFLEXTM BILIARY TRANSHEPATIC STE Boston Scientific Corporation
K122203 07/25/2012 TRUETOME BOSTON SCIENTIFIC CORP.
K102082 07/26/2010 EXTRACTOR PRO RX RETRIEVAL BALLONS, EXTRACTOR PRO XL RETRIEVAL BALLONS, EXTRACTOR PRO DL RETRIEVAL BALLONS MODEL M005470 BOSTON SCIENTIFIC CORP.


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