IQ-UIP is an AI-enabled medical device from Imbio, Inc., listed by FDA (510(k), K242467) with a decision date of 2024-12-19. Review panel: Radiology.
| FDA submission number | K242467 |
|---|---|
| Pathway | 510(k) |
| Company | Imbio, Inc. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2024-12-19 |
| Decision | Substantially Equivalent |
| Product code | QWO |
| Classification | Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease. |
| Device class | 2 |
| Regulation number | 892.2085 |
| Review time (calendar days) | 121 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
More devices from Imbio, Inc. · All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.