FDA 510(k) Application Details - K143609

Device Classification Name	Catheter, Biliary, Diagnostic   More FDA Info for this Device
510(K) Number	K143609
Device Name	Catheter, Biliary, Diagnostic
Applicant	OLYMPUS SURGICAL TECHNOLOGIES AMERICA 136 TURNPIKE ROAD SOUTHBOROUGH, MA 01772-2104 US Other 510(k) Applications for this Company
Contact	MARY ANNE PATELLA Other 510(k) Applications for this Contact
Regulation Number	876.5010   More FDA Info for this Regulation Number
Classification Product Code	FGE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/19/2014
Decision Date	03/27/2015
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