FDA 510(k) Applications Submitted by PEGGY KEIFFER

FDA 510(k) Number Submission Date Device Name Applicant
K030255 01/24/2003 SILICONE DUAL LUMEN RADPICC CATHETERS C.R. BARD, INC.
K010567 02/26/2001 OPTIFLOW CATHETER #5641190 CATHETER ONLY #5643150 CATHETER KIT #5631000 CATHETERLESS TRAY-GENERIC (COMBINED WITH CATHETR C.R. BARD, INC.
K010778 03/15/2001 NIAGARA SLIM-CATH C.R. BARD, INC.
K011015 04/04/2001 CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000 C.R. BARD, INC.
K031129 04/09/2003 POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC C.R. BARD, INC.
K050931 04/14/2005 6 FR DL POWERPICC CATHETER C.R. BARD, INC.
K051417 06/01/2005 6 FR FL POWERHOHN AND POWERLINE CATHETER C.R. BARD, INC.
K981994 06/08/1998 VASCATH OPTI-FLOW LONG TERM DUAL LUMEN HEMODIALYSIS CATHETER C.R. BARD, INC.
K022561 08/02/2002 CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000 C.R. BARD, INC.
K023374 10/08/2002 GROSHONG NXT DUAL LUMEN PICC CATHETERS C.R. BARD, INC.
K964066 10/10/1996 DUAL SLIM PORT IMPLANTED PORT (0654970/0654940) C.R. BARD, INC.
K063446 11/15/2006 CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000 C.R. BARD, INC.
K034020 12/24/2003 GROSHONG NXT PICC CATHETERS C.R. BARD, INC.


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