510(k) K881853 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
FRANZ CATHETER
| Applicant | Ep Technologies, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | May 3, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881853
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.