FDA 510(k) Applications Submitted by TERRI MORRIS

FDA 510(k) Number Submission Date Device Name Applicant
K050688 03/17/2005 TEGRESS IMPLANT NEEDLE C.R. BARD, INC.
K090739 03/20/2009 BARD SACROCOLPOPEXY GRAFT C.R. BARD, INC.
K120926 03/27/2012 ENDOBEAM HOLMIUM LASER FIBERS C.R. BARD, INC.
K080944 04/03/2008 X-FORCE NEPHROSTOMY BALLOON DILATION CATHETER C.R. BARD, INC.
K063632 12/06/2006 X-FORCE N30 NEPHROSTOMY BALLOON DILATION CATHETER C.R. BARD, INC.
K083839 12/23/2008 AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM, AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM C.R. BARD, INC.


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