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FDA 510(k) Applications for Medical Device Product Code "QWO"
FDA 510(k) Number
Applicant
Device Name
Decision Date
K242467
Imbio, Inc.
IQ-UIP
12/19/2024
DEN220040
Imvaria, Inc
Fibresolve
01/12/2024
K241891
Imvaria, Inc
ScreenDx
01/10/2025
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