CASSIE is an AI-enabled medical device from Wesper, Inc., listed by FDA (510(k), K252628) with a decision date of 2026-04-27. Review panel: Anesthesiology.
| FDA submission number | K252628 |
|---|---|
| Pathway | 510(k) |
| Company | Wesper, Inc. |
| Review panel (specialty) | Anesthesiology |
| FDA decision date | 2026-04-27 |
| Decision | Substantially Equivalent |
| Product code | MNR |
| Classification | Ventilatory Effort Recorder |
| Device class | 2 |
| Regulation number | 868.2375 |
| Review time (calendar days) | 250 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
All Anesthesiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.