FDA 510(k) Application Details - K091767

Device Classification Name	Catheter, Retention Type, Balloon   More FDA Info for this Device
510(K) Number	K091767
Device Name	Catheter, Retention Type, Balloon
Applicant	COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. SPENCER, IN 47460 US Other 510(k) Applications for this Company
Contact	BRENDA DAVIS Other 510(k) Applications for this Contact
Regulation Number	876.5130   More FDA Info for this Regulation Number
Classification Product Code	EZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/2009
Decision Date	10/09/2009
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