FDA 510(k) Applications Submitted by Exo Inc

FDA 510(k) Number Submission Date Device Name Applicant
K230497 02/24/2023 Bladder AI (AIBV01) Exo Inc
K232501 08/17/2023 AI Platform (AIP001) Exo Inc
K242359 08/09/2024 Strain AI (SAI001) Exo Inc
K243239 10/10/2024 Lung AI (LAI001) Exo Inc


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