510(k) K203793 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
RithmID-SD Steerable Diagnostic Electrophysiology Catheter
| Applicant | Synaptic Medical Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Feb 14, 2022 |
| Received | Dec 28, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203793
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.