FDA 510(k) Application Details - K020952

Device Classification Name	More FDA Info for this Device
510(K) Number	K020952
Device Name	SURX RF SYSTEM
Applicant	SURX, INC. 2675 COLLIER CANYON RD. LIVERMORE, CA 94550 US Other 510(k) Applications for this Company
Contact	ALAN CURTIS Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	MUK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/25/2002
Decision Date	05/30/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review