LINQ II Insertable Cardiac Monitor is an AI-enabled medical device from Medtronic, Inc., listed by FDA (510(k), K221962) with a decision date of 2022-08-25. Review panel: Cardiovascular.
| FDA submission number | K221962 |
|---|---|
| Pathway | 510(k) |
| Company | Medtronic, Inc. |
| Review panel (specialty) | Cardiovascular |
| FDA decision date | 2022-08-25 |
| Decision | Substantially Equivalent |
| Product code | MXD |
| Classification | Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection) |
| Device class | 2 |
| Regulation number | 870.1025 |
| Review time (calendar days) | 51 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
More devices from Medtronic, Inc. · All Cardiovascular AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.