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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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