FDA 510(k) Application Details - K023706

Device Classification Name	Unit, Electrosurgical, Endoscopic (With Or Without Accessories)   More FDA Info for this Device
510(K) Number	K023706
Device Name	Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Applicant	ULTROID, LLC 2230 DAMON RD. CARSON CITY, NV 89701 US Other 510(k) Applications for this Company
Contact	RONALD R NEWTON Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	KNS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/04/2002
Decision Date	01/14/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review