510(k) K190132 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter
| Applicant | Medtronic, Mounds View MN, US |
| Decision | Substantially Equivalent, Jul 30, 2019 |
| Received | Jan 28, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190132
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.