EndeavorRx— 510(k) DEN200026
UnknownAkili Interactive Labs, Inc.
FDA 510(k) clearance DEN200026 for EndeavorRx, Unknown on 2020-06-15. Applicant: Akili Interactive Labs, Inc.. Device class: 2.
Clearance details
- Applicant
- Akili Interactive Labs, Inc.
- Product code
- Code QFT
- Device class
- Class 2
- Regulation
- 21 CFR 882.5803
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Boston, MA, US
Recent devices under product code QFT
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