FDA 510(k) Applications for Medical Device Product Code "QUU"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K232545 | First Light Diagnostics, Inc. | The SensiTox B. anthracis Toxin Test | 11/20/2023 |
| DEN220044 | InBios International, Inc. | Active Anthrax DetectTM Plus Rapid Test | 02/03/2023 |
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