FDA 510(k) Application Details - K022979

Device Classification Name	Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)   More FDA Info for this Device
510(K) Number	K022979
Device Name	Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Applicant	INSTRUMENTS MEDICAUX G.B., INC. 1184 BLVD. ALEXANDRE SHERBROOKE, QUEBEC CA Other 510(k) Applications for this Company
Contact	MARTIN PAQUETTE 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	09/09/2002
Decision Date	12/18/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review