FDA 510(k) Application Details - K052009

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K052009
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	CONMED CORPORATION 14603 E. FREMONT AVE. CENTENNIAL, CO 80112 US Other 510(k) Applications for this Company
Contact	PAMELA VETTER 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	07/25/2005
Decision Date	09/28/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review