FDA 510(k) Application Details - K120147

Device Classification Name	Endoscopic Tissue Approximation Device   More FDA Info for this Device
510(K) Number	K120147
Device Name	Endoscopic Tissue Approximation Device
Applicant	BAROSENSE, INC 250 CHESAPEAKE DRIVE REDWOOD CITY, CA 94063 US Other 510(k) Applications for this Company
Contact	SHEILA STEVENS, PHD Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	OCW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/18/2012
Decision Date	02/17/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review