Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert is an AI-enabled medical device from GE Healthcare, listed by FDA (510(k), K213642) with a decision date of 2022-01-13. Review panel: Radiology.
| FDA submission number | K213642 |
|---|---|
| Pathway | 510(k) |
| Company | GE Healthcare |
| Review panel (specialty) | Radiology |
| FDA decision date | 2022-01-13 |
| Decision | Substantially Equivalent |
| Product code | IYN |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Device class | 2 |
| Regulation number | 892.1550 |
| Review time (calendar days) | 56 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
More devices from GE Healthcare · All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.