Circadia Technologies, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K234003 | The Circadia C200 System | May 30, 2024 |
| K200445 | The C100 Contactless Breathing Monitor | June 24, 2020 |