FDA 510(k) Application Details - K152853

Device Classification Name Catheter, Biliary, Diagnostic

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510(K) Number K152853
Device Name Catheter, Biliary, Diagnostic
Applicant BOSTON SCIENTIFIC CORP.
ONE SCIMED PLACE
MAPLE GROVE, MN 55311-1566 US
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Contact CARAH KUCHARSKI
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Regulation Number 876.5010

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Classification Product Code FGE
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Date Received 09/29/2015
Decision Date 11/20/2015
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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