FDA 510(k) Application Details - K962313

Device Classification Name	Electrode, Electrosurgical   More FDA Info for this Device
510(K) Number	K962313
Device Name	Electrode, Electrosurgical
Applicant	RADIOTHERAPEUTICS CORP. 2680 BAYSHORE PKWY. SUITE 106 MOUNTAIN VIEW, CA 94043 US Other 510(k) Applications for this Company
Contact	COLIN J NICHOLS Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	JOS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/1996
Decision Date	09/11/1996
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