Rapid LVO is an AI-enabled medical device from iSchemaView Inc., listed by FDA (510(k), K221248) with a decision date of 2022-05-31. Review panel: Radiology.
| FDA submission number | K221248 |
|---|---|
| Pathway | 510(k) |
| Company | iSchemaView Inc. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2022-05-31 |
| Decision | Substantially Equivalent |
| Product code | QAS |
| Classification | Radiological Computer-Assisted Triage And Notification Software |
| Device class | 2 |
| Regulation number | 892.2080 |
| Review time (calendar days) | 29 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
More devices from iSchemaView 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.