510(k) K940168 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
DIAGNOSTIC II CATHETER
| Applicant | Ep Technologies, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jul 27, 1994 |
| Received | Jan 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940168
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.