FDA 510(k) Applications Submitted by WAYNE R HOHMAN

FDA 510(k) Number Submission Date Device Name Applicant
K093376 10/29/2009 LASSO NAV CATHETER BIOSENSE WEBSTER, INC.
K050217 01/31/2005 FLOWER HIGH-DENSITY MAPPING CATHETER, 4-4-4 MM ELECTRODE SPACING), (2-6-2 MM ELECTRODE SPACING) BIOSENSE WEBSTER, INC.
K120425 02/13/2012 PENTARAY NAV HIGH-DENSITY MAPPING CATHETER BIOSENSE WEBSTER, INC.
K120550 02/23/2012 CARTO(R) EP NAVIGATION SYSTEM, VERSION 3.0 (WITH STANDARD LOCATION PAD) BIOSENSE WEBSTER, INC.
K972142 06/06/1997 ACS HI-TORQUE ALL STAR 0.014 GUIDE WIRE WITH MICROGLIDE COATING GUIDANT CORP.
K112007 07/14/2011 CARTO 3 EP NAVIGATION SYSTEM, VERSION 2.2 BIOSENSE WEBSTER, INC.
K953564 07/31/1995 MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE MEDTRONIC CARDIAC SURGERY, MEDTRONIC, INC.
K132782 09/06/2013 CARTO3 EP NAVIGATION SYSTEM, VERSION 3.2 BIOSENSE WEBSTER, INC.
K093566 11/18/2009 CARTO XP EP NAVIGATION SYSTEM, VERSION 10 BIOSENSE WEBSTER, INC.
K123837 12/13/2012 PENTARAY NAV ECO HIGH-DENSITY MAPPING CATHETER BIOSENSE WEBSTER, INC.
K103746 12/23/2010 CARTO 3 EP NAVIGATION SYSTEM, VERSION 2.0 (W/STANDARD LOCATION PAD),CARTO3 EPNAVIGATION SYSTEM,VERSION 2.0 W/RMT PAD) BIOSENSE WEBSTER, INC.
K133916 12/23/2013 CARTO 3 EP NAVIGATION SYSTEM, VERSION 4.2 BIOSENSE WEBSTER, INC.


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