| K-number | K231337 |
| Device name | EndeavorRx |
| Applicant | Akili Interactive Labs, Inc. |
| Product code | QFT |
| Device class | Class II |
| Decision date | Dec 13, 2023 |
| Decision | Substantially Equivalent |
| Regulation | 882.5803 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov