FDA 510(k) Application Details - K961702

Device Classification Name	Electrode, Electrosurgical, Active, Urological   More FDA Info for this Device
510(K) Number	K961702
Device Name	Electrode, Electrosurgical, Active, Urological
Applicant	KARL STORZ ENDOSKOP GMBH 600 CORPORATE POINTE CULVER CITY, CA 90230 US Other 510(k) Applications for this Company
Contact	BETTY M JOHNSON Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	FAS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/02/1996
Decision Date	08/29/1996
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