FDA 510(k) Application Details - K962593

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K962593
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	XIMED/PROSURE/INJECTX 2195 TRADE ZONE BLVD. SAN JOSE, CA 95131 US Other 510(k) Applications for this Company
Contact	ASHVIN DESAI 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	07/02/1996
Decision Date	11/12/1996
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