First Light Diagnostics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232545 | The SensiTox B. anthracis Toxin Test | November 20, 2023 |
| K193490 | SensiTox C. difficile Toxin Test | July 8, 2021 |