FDA 510(k) Applications Submitted by MARION GORDON

FDA 510(k) Number Submission Date Device Name Applicant
K990504 02/17/1999 MEMOTHERM COLORECTAL STENT C.R. BARD, INC.
K991375 04/21/1999 BARD BALLOON INFLATION SYSTEM C.R. BARD, INC.
K002094 07/11/2000 BARD MEMOTHERM COVERED ESOPHAGEAL STENT, MODEL MULTIPLE C.R. BARD, INC.
K982557 07/22/1998 BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES BARD INTERVENTIONAL PRODUCTS DIV.
K973500 09/16/1997 BARD ENDOSCOPIC OVERTUBE (#000307) C.R. BARD, INC.
K013144 09/20/2001 DUAL PORT WIZARD LOW PROFILE REPLACEMENT GASTROSTOMY DEVICE; DUAL PORT WIZARD FEEDING/DECOMPRESSION TUBE, MODEL 00220W C.R. BARD, INC.
K993892 11/16/1999 DURAGLIDE STONE REMOVAL BALLOON, MODEL 000635-38, 000646-47, DURAGLIDE STONE BALLOON, MODEL 007124-25,007144-45 C.R. BARD, INC.
K040542 03/02/2004 SMITH & NEPHEW GTS SLEEVE AND GTS TAPERED SCREW SMITH & NEPHEW, INC.
K131038 04/15/2013 NMI PICC MAXIMAL BARRIER NURSING KITS NAVILYST MEDICAL, INC.
K121990 07/06/2012 PICC CONVENIENCE KIT NAVILYST MEDICAL, INC.
K032224 07/21/2003 BIORCI SCREW SMITH & NEPHEW, INC.
K113198 10/31/2011 NMI CONTROL SYRINGE, 7 ML NMI CONTROL SYRINGE, 8 ML NAVILYST MEDICAL, INC.


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