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First Light Diagnostics, Inc.

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

Total Devices2
Categories2
Latest Approval2023-11-20
TypeNumberDevice NameCodeDate
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
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