510(k) K252794 · DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Vision-MR Diagnostic Catheter
| Applicant | Imricor Medical Systems, Inc., Burnsville MN, US |
| Decision | Substantially Equivalent, Jan 8, 2026 |
| Received | Sep 2, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252794
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.