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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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