SmartTarget is an AI-enabled medical device from SmartTarget, Ltd., listed by FDA (510(k), K170250) with a decision date of 2017-06-07. Review panel: Radiology.
| FDA submission number | K170250 |
|---|---|
| Pathway | 510(k) |
| Company | SmartTarget, Ltd. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2017-06-07 |
| Decision | Substantially Equivalent |
| Product code | LLZ |
| Classification | System, Image Processing, Radiological |
| Device class | 2 |
| Regulation number | 892.2050 |
| Review time (calendar days) | 131 |
| Applicant country | GB |
Official FDA database record · FDA AI-enabled device list
All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.