Clarius Ultrasound System is an AI-enabled medical device from Clarius Mobile Health Corp., listed by FDA (510(k), K172385) with a decision date of 2017-09-14. Review panel: Radiology.
| FDA submission number | K172385 |
|---|---|
| Pathway | 510(k) |
| Company | Clarius Mobile Health Corp. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2017-09-14 |
| Decision | Substantially Equivalent |
| Product code | IYN |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Device class | 2 |
| Regulation number | 892.1550 |
| Review time (calendar days) | 37 |
| Applicant country | CA |
Official FDA database record · FDA AI-enabled device list
More devices from Clarius Mobile Health Corp. · All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.