FDA 510(k) Application Details - K003773

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K003773
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	WEBB RESEARCH II, INC. 1241 CARPENTER ST. PHILADELPHIA, PA 19147 US Other 510(k) Applications for this Company
Contact	STEVEN KRUPNICK 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	12/06/2000
Decision Date	02/02/2001
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