Medical Device Manufacturer · US , Boston , MA

Akili Interactive Labs, Inc. - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 2020

Total

Cleared

Denied

Akili Interactive Labs, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boston, US.

Latest FDA clearance: Jun 2024. Active since 2020. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Akili Interactive Labs, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Akili Interactive Labs, Inc.

3 devices

1-3 of 3