StrokeViewer Perfusion is an AI-enabled medical device from NICo-Lab B.V., listed by FDA (510(k), K231570) with a decision date of 2023-12-14. Review panel: Radiology.
| FDA submission number | K231570 |
|---|---|
| Pathway | 510(k) |
| Company | NICo-Lab B.V. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2023-12-14 |
| Decision | Substantially Equivalent |
| Product code | LLZ |
| Classification | System, Image Processing, Radiological |
| Device class | 2 |
| Regulation number | 892.2050 |
| Review time (calendar days) | 197 |
| Applicant country | NL |
Official FDA database record · FDA AI-enabled device list
More devices from NICo-Lab B.V. · All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.