FDA 510(k) Applications Submitted by NATALIE BENNINGTON

FDA 510(k) Number Submission Date Device Name Applicant
K030429 02/10/2003 STERRAD 200 STERILIZER ADVANCED STERILIZATION PRODUCTS
K090898 04/01/2009 CORONARY SINUS DEFLECTABLE MAPPING CATHETER, MODEL D-1263-01, WEBSTER CS CATHETER WITH EZ STEER BIOSENSE WEBSTER, INC.
K031226 04/18/2003 STERRAD CYCLESURE BIOLOGICAL INDICATOR ADVANCED STERILIZATION PRODUCTS
K081258 05/02/2008 VARIABLE LASSO NAV CATHETER, MODELS: D-1290-01, D-1290-02 BIOSENSE WEBSTER, INC.
K061463 05/26/2006 ESOPHAGEAL MAPPING CATHETER, MODEL D-1272-01-S BIOSENSE WEBSTER, INC.
K061468 05/26/2006 REFSTAR EXTERNAL REFERENCE PATCH BIOSENSE WEBSTER, INC.
K022441 07/25/2002 STERRAD SEALSURE CHEMICAL INDICATOR TAPE ADVANCED STERILIZATION PRODUCTS
K042116 08/05/2004 STERRAD NX STERILIZER ADVANCED STERILIZATION PRODUCTS
K072202 08/08/2007 CARTO 3 NAVIGATION SYSTEM (MODEL:FG-5400-00), CARTO 3 EXTERNAL REFERENCE PATCHES (MODEL:D-1283-01) BIOSENSE WEBSTER, INC.
K013003 09/06/2001 APTIMAX INSTRUMENT TRAY, INSTRUMENT MAT AND INSTRUMENT HOLDER ADVANCED STERILIZATION PRODUCTS
K023290 10/02/2002 STERRAD 50 & STERRAD 100S STERILIZERS ADVANCED STERILIZATION PRODUCTS


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