510(k) K162892 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Achieve Advance Mapping Catheter
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Nov 15, 2016 |
| Received | Oct 17, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162892
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.