Lumos 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 |
|---|
| K260787 | FebriDx Bacterial/Non-bacterial Assay | March 24, 2026 |
| K230917 | FebriDx Bacterial / Non-bacterial Point of Care Assay | June 30, 2023 |