510(k) K240366 · DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
EPXT Unidirectional Steerable Diagnostic Catheter; Dynamic Tip Unidirectional Steerable Diagnostic Catheter; Dynamic XT Unidirectional Steerable Diagnostic Catheter
| Applicant | Boston Scientific Corporation, St Paul MN, US |
| Decision | Substantially Equivalent, Nov 1, 2024 |
| Received | Feb 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240366
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.