FDA 510(k) Application Details - K092090

Device Classification Name	Endoscopic Injection Needle, Gastroenterology-Urology   More FDA Info for this Device
510(K) Number	K092090
Device Name	Endoscopic Injection Needle, Gastroenterology-Urology
Applicant	BYRNE MEDICAL INC. 3150 POLLOK DR CONROE, TX 77303 US Other 510(k) Applications for this Company
Contact	CHRIS HIERHOLZER Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FBK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/14/2009
Decision Date	11/30/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review