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Exo, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K243239 Lung AI (LAI001)MYN2025-04-24 View
510(k) K242359 Strain AI (SAI001)QIH2024-11-20 View
510(k) K232501 AI Platform (AIP001)QIH2023-11-17 View
510(k) K230497 Bladder AI (AIBV01)QIH2023-06-22 View
510(k) K831801 HEMOCLAV VENOUS CATHETERFIQ1983-07-07 View
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