510(k) K971975 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CARDIMA PATHFINDER 1.5F MAPPING MICROCATHETER
| Applicant | Cardima, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Jul 1, 1998 |
| Received | May 29, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971975
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.