First Light Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-11-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232545 | The SensiTox B. anthracis Toxin Test | QUU | 2023-11-20 | View |
| 510(k) | K193490 | SensiTox C. difficile Toxin Test | LLH | 2021-07-08 | View |
No matching devices.