FDA 510(k) Application Details - K110518

Device Classification Name	Collector, Urine, (And Accessories) For Indwelling Catheter   More FDA Info for this Device
510(K) Number	K110518
Device Name	Collector, Urine, (And Accessories) For Indwelling Catheter
Applicant	FUTURE PATH MEDICAL, LLC 8870 RAVELLO CT NAPLES, FL 34114 US Other 510(k) Applications for this Company
Contact	DANIEL KAMM Other 510(k) Applications for this Contact
Regulation Number	876.5250   More FDA Info for this Regulation Number
Classification Product Code	KNX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/23/2011
Decision Date	06/24/2011
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