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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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