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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