510(k) K160689 ยท MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
Reveal LINQ
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Apr 22, 2016 |
| Received | Mar 11, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160689
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.