510(k) K233900 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Nordica PV Cryo Mapping Catheter
| Applicant | Synaptic Medical Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 6, 2024 |
| Received | Dec 11, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233900
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.