510(k) K900765 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
STEEROCATH(TM)
| Applicant | Ep Technologies, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, May 7, 1990 |
| Received | Feb 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900765
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.