510(k) K230503 · DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Polaris X Catheter Cable, Blazer Dx-20 Catheter Cable
| Applicant | Boston Scientific, St Paul MN, US |
| Decision | Substantially Equivalent, Apr 25, 2023 |
| Received | Feb 24, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230503
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.