MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile is an AI-enabled medical device from Siemens Healthcare GmbH, listed by FDA (510(k), K250443) with a decision date of 2025-06-16. Review panel: Radiology.
| FDA submission number | K250443 |
|---|---|
| Pathway | 510(k) |
| Company | Siemens Healthcare GmbH |
| Review panel (specialty) | Radiology |
| FDA decision date | 2025-06-16 |
| Decision | Substantially Equivalent |
| Product code | LNH |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Device class | 2 |
| Regulation number | 892.1000 |
| Review time (calendar days) | 122 |
| Applicant country | DE |
Official FDA database record · FDA AI-enabled device list
More devices from Siemens Healthcare GmbH · All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.