Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) is an AI-enabled medical device from Varian Medical Systems Inc., listed by FDA (510(k), K232923) with a decision date of 2024-04-30. Review panel: Radiology.
| FDA submission number | K232923 |
|---|---|
| Pathway | 510(k) |
| Company | Varian Medical Systems Inc. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2024-04-30 |
| Decision | Substantially Equivalent |
| Product code | IYE |
| Classification | Accelerator, Linear, Medical |
| Device class | 2 |
| Regulation number | 892.5050 |
| Review time (calendar days) | 224 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
More devices from Varian Medical Systems Inc. · All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.