FDA 510(k) Application Details - K132619

Device Classification Name	Catheter, Straight   More FDA Info for this Device
510(K) Number	K132619
Device Name	Catheter, Straight
Applicant	FLEXICARE MEDICAL LTD. CYNON VALLEY BUSINESS PARK MOUTAIN ASH MID GLAMORGAN CF45 4ER GB Other 510(k) Applications for this Company
Contact	CHRISTOPHER WATKINS Other 510(k) Applications for this Contact
Regulation Number	876.5130   More FDA Info for this Regulation Number
Classification Product Code	EZD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/21/2013
Decision Date	10/11/2013
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