Cardima, Inc.
FDA 510(k) & PMA Approved Devices — 12 products
Advertisement
Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K060715 | MODIFICATION TO: CARDIMA ABLATION SYSTEM | OCL | 2006-05-15 | View |
| 510(k) | K022008 | CARDIMA ABLATION SYSTEM | OCL | 2003-01-29 | View |
| 510(k) | K974683 | NAVIPORT DEFLECTABLE TIP GUIDING CATHETER | DQY | 1999-06-22 | View |
| 510(k) | K972803 | TRACER O-T-W MAPPING DEVICE | DRF | 1999-05-11 | View |
| 510(k) | K982835 | ELECTRODE SWITCHBOX, MODEL 11-081002 | DRF | 1998-10-29 | View |
| 510(k) | K971975 | CARDIMA PATHFINDER 1.5F MAPPING MICROCATHETER | DRF | 1998-07-01 | View |
| 510(k) | K973298 | CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER | DQY | 1998-06-26 | View |
| 510(k) | K970853 | PATHFINDER 3MM MAPPING MICROCATHETER (01-082001) | DRF | 1997-11-04 | View |
| 510(k) | K955802 | PATHFINDER | DRF | 1997-01-29 | View |
| 510(k) | K951603 | CARDIMA, INC. FORERUNNER | DQY | 1995-10-05 | View |
| 510(k) | K932800 | CARDIMA TRACKER(R) INFUSION CATHETER | KRA | 1993-12-21 | View |
| 510(k) | K932801 | CARDIMA SEEKER AND STUBBIE GUIDEWIRES | DQX | 1993-09-01 | View |
No matching devices.
Advertisement