510(k) K955802 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
PATHFINDER
| Applicant | Cardima, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Jan 29, 1997 |
| Received | Dec 22, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955802
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.