510(k) K163460 ยท MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
Reveal LINQ Insertable Cardiac Monitor
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Feb 14, 2017 |
| Received | Dec 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163460
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.