FDA 510(k) Applications Submitted by CARDIMA, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K060715 |
03/17/2006 |
MODIFICATION TO: CARDIMA ABLATION SYSTEM |
CARDIMA, INC. |
| K955802 |
12/22/1995 |
PATHFINDER |
CARDIMA, INC. |
| K971975 |
05/29/1997 |
CARDIMA PATHFINDER 1.5F MAPPING MICROCATHETER |
CARDIMA, INC. |
| K982835 |
08/12/1998 |
ELECTRODE SWITCHBOX, MODEL 11-081002 |
CARDIMA, INC. |
| K970853 |
03/07/1997 |
PATHFINDER 3MM MAPPING MICROCATHETER (01-082001) |
CARDIMA, INC. |
| K022008 |
06/19/2002 |
CARDIMA ABLATION SYSTEM |
CARDIMA, INC. |
| K972803 |
07/28/1997 |
TRACER O-T-W MAPPING DEVICE |
CARDIMA, INC. |
| K973298 |
09/02/1997 |
CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER |
CARDIMA, INC. |
| K974683 |
12/16/1997 |
NAVIPORT DEFLECTABLE TIP GUIDING CATHETER |
CARDIMA, INC. |
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