FDA 510(k) Application Details - K011220

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K011220
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	RADIOTHERAPEUTICS CORP. 1308 BORREGAS AVE.SUITE 200 SUNNYVALE, CA 94089 US Other 510(k) Applications for this Company
Contact	GARY CURTIS 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	04/20/2001
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	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review