Circadia Technologies, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-05-30
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K234003 | The Circadia C200 System | DRT | 2024-05-30 | View |
| 510(k) | K200445 | The C100 Contactless Breathing Monitor | BZQ | 2020-06-24 | View |
No matching devices.