FDA 510(k) Application Details - K022561

Device Classification Name	Kit, Repair, Catheter, Hemodialysis   More FDA Info for this Device
510(K) Number	K022561
Device Name	Kit, Repair, Catheter, Hemodialysis
Applicant	C.R. BARD, INC. 5425 WEST AMELIA EARHART DR. SALT LAKE CITY, UT 84116 US Other 510(k) Applications for this Company
Contact	PEGGY KEIFFER Other 510(k) Applications for this Contact
Regulation Number	876.5540   More FDA Info for this Regulation Number
Classification Product Code	NFK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/02/2002
Decision Date	08/23/2002
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