510(k) K232651 · DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
BLAZER Dx-20 Bidirectional Steerable Diagnostic Catheter
| Applicant | Boston Scientific Corporation, St Paul MN, US |
| Decision | Substantially Equivalent, Sep 29, 2023 |
| Received | Aug 31, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232651
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.