FDA 510(k) Application Details - K021079

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K021079
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	CONMED CORP. 14603 E. FREMONT AVE. CENTENNIAL, CO 80112 US Other 510(k) Applications for this Company
Contact	CHARLES M HART Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/03/2002
Decision Date	07/01/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review