FDA 510(k) Applications Submitted by JOHN KNORPP

FDA 510(k) Number Submission Date Device Name Applicant
K070879 03/30/2007 BARD MALECOT AND PEZZER DRAINS C.R. BARD, INC.
K093747 12/04/2009 ALIGN AND ALIGN TO URETHRAL SUPPORT SYSTEMS C.R. BARD, INC.
K040504 02/27/2004 BARDEX, LUBRI-SIL AND LUBRI-SIL IC ALL-SILICONE FOLEY CATHETERS C.R. BARD, INC.
K040658 03/12/2004 BARDEX I.C. LATEX FOLEY CATHETER C.R. BARD, INC.
K050875 04/06/2005 U-BALLOON DILATION CATHETER C.R. BARD, INC.
K051316 05/20/2005 X-FORCE NEPHROSTOMY BALLOON DILATION CATHETER C.R. BARD, INC.
K111611 06/09/2011 ENDOMAXX FULLY COVERED ESOPHAGEAL STENT MERIT MEDICAL SYSTEMS, INC.
K041576 06/11/2004 SOURCELINK C.R. BARD, INC.
K032044 07/02/2003 X-PROT DUO PORT C.R. BARD, INC.
K092607 08/25/2009 AJUST ADJUSTABLE SINGLE INCISION SLING C.R. BARD, INC.
K082571 09/05/2008 AVAULTA SUPPORT SYSTEM C.R. BARD, INC.
K022983 09/09/2002 BARDPORT X-PORT ISP PORT C.R. BARD, INC.
K042949 10/26/2004 PELVILACE TRANSOBTURATOR BIOURETHRAL SUPPORT SYSTEM (PELVILACE TO SYSTEM) C.R. BARD, INC.
K043246 11/23/2004 BRACHYSOURCE BRACHYTHERAPY SEED IMPLANTS C.R. BARD, INC.
K063712 12/14/2006 AVAULTA SUPPORT SYSTEM/AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM C.R. BARD, INC.


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