FDA 510(k) Application Details - K090102

Device Classification Name	Catheter, Hemodialysis, Non-Implanted   More FDA Info for this Device
510(K) Number	K090102
Device Name	Catheter, Hemodialysis, Non-Implanted
Applicant	C.R. BARD, INC. 605 N 5600 W SALT LAKE CITY, UT 84116 US Other 510(k) Applications for this Company
Contact	JESSICA AGNELLO Other 510(k) Applications for this Contact
Regulation Number	876.5540   More FDA Info for this Regulation Number
Classification Product Code	MPB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/15/2009
Decision Date	02/12/2009
Decision	SEKD - SUBST EQUIV - KIT WITH DRUGS
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review