K233496
- 510(k) number
- K233496
- Device name
- EndeavorOTC
- Applicant
- Akili Interactive Labs, Inc. MA · US
- Product code
- QFT — Digital Therapeutic Software For Attention Deficit H
- Decision date
- 2024-06-14
- Date received
- 2023-10-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
510(k) Summary (official FDA PDF): K233496.pdf
Official FDA record: K233496
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.