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Median Technologies files FDA 513(g) regulatory submission for iBiopsy® Lung Cancer Screening CADe/CADx Software as Medical Device

Median Technologies files FDA 513(g) regulatory submission for iBiopsy® Lung Cancer Screening CADe/CADx Software as Medical Device  ·      513(g) submission is a key milestone that marks the initiation of Median’s interactions with the FDA.·  &nbsp. ....

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