KOSMOS is an AI-enabled medical device from EchoNous, Inc., listed by FDA (510(k), K193518) with a decision date of 2020-03-26. Review panel: Radiology.
| FDA submission number | K193518 |
|---|---|
| Pathway | 510(k) |
| Company | EchoNous, Inc. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2020-03-26 |
| Decision | Substantially Equivalent |
| Product code | IYN |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Device class | 2 |
| Regulation number | 892.1550 |
| Review time (calendar days) | 98 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
More devices from EchoNous, 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.