MEDO ARIA is an AI-enabled medical device from Medo.ai, listed by FDA (510(k), K200356) with a decision date of 2020-06-11. Review panel: Radiology.
| FDA submission number | K200356 |
|---|---|
| Pathway | 510(k) |
| Company | Medo.ai |
| Review panel (specialty) | Radiology |
| FDA decision date | 2020-06-11 |
| Decision | Substantially Equivalent |
| Product code | QIH |
| Classification | Automated Radiological Image Processing Software |
| Device class | 2 |
| Regulation number | 892.2050 |
| Review time (calendar days) | 119 |
| Applicant country | CA |
Official FDA database record · FDA AI-enabled device list
All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.