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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