510(k) K954651 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ELECTRODE RECORDING CATHETER
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Oct 22, 1996 |
| Received | Oct 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954651
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.