LungQ v3.0.0 is an AI-enabled medical device from Thirona BV, listed by FDA (510(k), K232412) with a decision date of 2024-01-08. Review panel: Radiology.
| FDA submission number | K232412 |
|---|---|
| Pathway | 510(k) |
| Company | Thirona BV |
| Review panel (specialty) | Radiology |
| FDA decision date | 2024-01-08 |
| Decision | Substantially Equivalent |
| Product code | JAK |
| Classification | System, X-Ray, Tomography, Computed |
| Device class | 2 |
| Regulation number | 892.1750 |
| Review time (calendar days) | 151 |
| Applicant country | NL |
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.