Nerveblox is an AI-enabled medical device from Smart Alfa Teknoloji San. Ve Tic. A.S., listed by FDA (510(k), K250818) with a decision date of 2025-08-15. Review panel: Anesthesiology.
| FDA submission number | K250818 |
|---|---|
| Pathway | 510(k) |
| Company | Smart Alfa Teknoloji San. Ve Tic. A.S. |
| Review panel (specialty) | Anesthesiology |
| FDA decision date | 2025-08-15 |
| Decision | Substantially Equivalent |
| Product code | QRG |
| Classification | Ultrasound Guided Nerve Block Assist |
| Device class | 2 |
| Regulation number | 868.1980 |
| Review time (calendar days) | 150 |
| Applicant country | TR |
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.