FDA 510(k) Application Details - K964594

Device Classification Name	Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)   More FDA Info for this Device
510(K) Number	K964594
Device Name	Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Applicant	CIRCON CORP. 300 STILLWATER AVE. STAMFORD, CT 06902-3695 US Other 510(k) Applications for this Company
Contact	ERVIN F TAYLOR, P.E. Other 510(k) Applications for this Contact
Regulation Number	884.4160   More FDA Info for this Regulation Number
Classification Product Code	KNF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/15/1996
Decision Date	08/15/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review