Lumos Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2026-03-24
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K260787 | FebriDx Bacterial/Non-bacterial Assay | QXA | 2026-03-24 | View |
| 510(k) | K230917 | FebriDx Bacterial / Non-bacterial Point of Care Assay | QXA | 2023-06-30 | View |
No matching devices.