FDA 510(k) Application Details - K090217

Device Classification Name	Endoscopic Injection Needle, Gastroenterology-Urology   More FDA Info for this Device
510(K) Number	K090217
Device Name	Endoscopic Injection Needle, Gastroenterology-Urology
Applicant	COLOPLAST A/S 1601 WEST RIVER ROAD N MINNEAPOLIS, MN 55411 US Other 510(k) Applications for this Company
Contact	SURESH GHAL 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	01/29/2009
Decision Date	04/23/2009
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	N
Expedited Review