Rapid is an AI-enabled medical device from iSchema View Inc., listed by FDA (510(k), K213165) with a decision date of 2022-02-08. Review panel: Radiology.
| FDA submission number | K213165 |
|---|---|
| Pathway | 510(k) |
| Company | iSchema View Inc. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2022-02-08 |
| Decision | Substantially Equivalent |
| Product code | LLZ |
| Classification | System, Image Processing, Radiological |
| Device class | 2 |
| Regulation number | 892.2050 |
| Review time (calendar days) | 133 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
More devices from iSchema View 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.