FDA 510(k) Application Details - K030268

Device Classification Name	Catheter, Hemodialysis, Non-Implanted   More FDA Info for this Device
510(K) Number	K030268
Device Name	Catheter, Hemodialysis, Non-Implanted
Applicant	C.R. BARD, INC. 5425 WEST AMELIA EARHART DR. SALT LAKE CITY, UT 84116 US Other 510(k) Applications for this Company
Contact	GLENN NORTON 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	01/27/2003
Decision Date	07/30/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review