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Lumos Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K260787 FebriDx Bacterial/Non-bacterial AssayQXA2026-03-24 View
510(k) K230917 FebriDx Bacterial / Non-bacterial Point of Care AssayQXA2023-06-30 View
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