510(k) K220796 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
IntellaMap Orion High Resolution Mapping Catheter
| Applicant | Boston Scientific Corporation, St Paul MN, US |
| Decision | Substantially Equivalent, Jun 10, 2022 |
| Received | Mar 18, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K220796
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.