510(k) K212008 ยท MXD Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
Reveal LINQ Insertable Cardiac Monitor
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Jul 22, 2021 |
| Received | Jun 28, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212008
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.