Spectral CT Verida Family is an AI-enabled medical device from Philips Medical Systems Technologies , Ltd., listed by FDA (510(k), K253649) with a decision date of 2026-03-27. Review panel: Radiology.
| FDA submission number | K253649 |
|---|---|
| Pathway | 510(k) |
| Company | Philips Medical Systems Technologies , Ltd. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2026-03-27 |
| Decision | Substantially Equivalent |
| Product code | JAK |
| Classification | System, X-Ray, Tomography, Computed |
| Device class | 2 |
| Regulation number | 892.1750 |
| Review time (calendar days) | 127 |
| Applicant country | IL |
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.