NeuroRPM is an AI-enabled medical device from New Touch Digital Inc., listed by FDA (510(k), K221772) with a decision date of 2023-03-17. Review panel: Neurology.
| FDA submission number | K221772 |
|---|---|
| Pathway | 510(k) |
| Company | New Touch Digital Inc. |
| Review panel (specialty) | Neurology |
| FDA decision date | 2023-03-17 |
| Decision | Substantially Equivalent |
| Product code | GYD |
| Classification | Transducer, Tremor |
| Device class | 2 |
| Regulation number | 882.1950 |
| Review time (calendar days) | 269 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
All Neurology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.