FDA 510(k) Application Details - K971939

Device Classification Name	Endoscopic Tissue Approximation Device   More FDA Info for this Device
510(K) Number	K971939
Device Name	Endoscopic Tissue Approximation Device
Applicant	SMITH & NEPHEW ENDOSCOPY, INC. 130 FORBES BLVD. MANSFIELD, MA 02048 US Other 510(k) Applications for this Company
Contact	AMY L WALTERS 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	05/27/1997
Decision Date	08/06/1997
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