FDA 510(k) Applications for Medical Device Product Code "QFT"

FDA 510(k) Number Applicant Device Name Decision Date
DEN200026 Akili Interactive Labs Inc. EndeavorRx 06/15/2020
K233496 Akili Interactive Labs, Inc. EndeavorOTC 06/14/2024
K231337 Akili Interactive Labs, Inc. EndeavorRx 12/13/2023
K243729 Lumos Labs, Inc. Prismira 06/13/2025


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