510(k) K970853 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
PATHFINDER 3MM MAPPING MICROCATHETER (01-082001)
| Applicant | Cardima, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Nov 4, 1997 |
| Received | Mar 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970853
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.