510(k) K953750 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Mar 11, 1996 |
| Received | Aug 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953750
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.