510(k) K924108 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
TRACFINDER II
| Applicant | Ep Technologies, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Dec 16, 1993 |
| Received | Aug 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924108
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.