FDA 510(k) Applications Submitted by SANDRA L PERREAND

FDA 510(k) Number Submission Date Device Name Applicant
K030328 01/31/2003 VIDAS D-DIMER NEW (DD2) ASSAY, MODEL 30 442 BIOMERIEUX, INC.
K990514 02/18/1999 MODIFICATION OF BARD QUANTUM CVR, MODEL H-6770VR C.R. BARD, INC.
K980850 03/05/1998 BARD 9FR., 40CC. REDIGUARD AND TAPERSEAL INTRA-AORTIC BALLOONS C.R. BARD, INC.
K020810 03/13/2002 VIDAS D-DIMER NEW (DD2) ASSAY MODEL#30 442 BIOMERIEUX, INC.
K040882 04/05/2004 VIDAS D-DIMER EXCLUSION ASSAY, MODEL 30 442 BIOMERIEUX, INC.
K981660 05/11/1998 Bard 8 Fr., 40cc. & 7Fr., 30cc Intra-Aortic Balloon Catheters C.R. BARD, INC.
K973962 10/16/1997 BARD 9FR., 30CC REDIGUARD AND TAPERSEAL BALLOONS C.R. BARD, INC.
K063261 10/30/2006 NUCLISENS EASYQ ENTEROVIRUS SYSTEM BIOMERIEUX, INC.
K113200 10/31/2011 VITEK 2 AST-GN PIPERACILLIN/TAZOBACTAM BIOMERIEUX, INC.
K080561 02/28/2008 VIDAS CA 125 II ASSAY BIOMERIEUX, INC.
K961134 03/21/1996 BARD GRAFT SIZER C.R. BARD, INC.
K971180 03/31/1997 BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT C.R. BARD, INC.
K971421 04/16/1997 BARD ISOFLOW BLOOD PUMP C.R. BARD, INC.
K962177 06/06/1996 BARD TAPERSEAL INTRA-AORTIC BALLOON CATHETER & INTRODUCER KIT C.R. BARD, INC.


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