LumiNE US; Lumi is an AI-enabled medical device from Augmedit B.V., listed by FDA (510(k), K240094) with a decision date of 2024-09-10. Review panel: Radiology.
| FDA submission number | K240094 |
|---|---|
| Pathway | 510(k) |
| Company | Augmedit B.V. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2024-09-10 |
| Decision | Substantially Equivalent |
| Product code | QIH |
| Classification | Automated Radiological Image Processing Software |
| Device class | 2 |
| Regulation number | 892.2050 |
| Review time (calendar days) | 242 |
| Applicant country | NL |
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.