LOGIQ Fortis is an AI-enabled medical device from GE Medical Systems Ultrasound and Primary Care Diagnostics, listed by FDA (510(k), K253366) with a decision date of 2026-01-07. Review panel: Radiology.
| FDA submission number | K253366 |
|---|---|
| Pathway | 510(k) |
| Company | GE Medical Systems Ultrasound and Primary Care Diagnostics |
| Review panel (specialty) | Radiology |
| FDA decision date | 2026-01-07 |
| Decision | Substantially Equivalent |
| Product code | IYN |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Device class | 2 |
| Regulation number | 892.1550 |
| Review time (calendar days) | 99 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
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Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.