510(k) K183547 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Marinr Steerable Intracardiac Electrode Catheter, StableMapr Steerable Intracardiac Electrode Catheter, Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter
| Applicant | Medtronic, Mounds View MN, US |
| Decision | Substantially Equivalent, Jul 30, 2019 |
| Received | Dec 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183547
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.