FDA 510(k) Application Details - K100686

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K100686
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	SHAWN RIEDEL 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	03/10/2010
Decision Date	05/21/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review