510(k) K211375 · 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 10, 2021 |
| Received | May 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211375
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.