Canvas Dx— 510(k) K243558
Substantially EquivalentCognoa, Inc.
FDA 510(k) clearance K243558 for Canvas Dx, Substantially Equivalent on 2025-04-11. Applicant: Cognoa, Inc.. Device class: 2.
Clearance details
- Applicant
- Cognoa, Inc.
- Product code
- Code QPF
- Device class
- Class 2
- Regulation
- 21 CFR 882.1491
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palo Alto, CA, US
Recent devices under product code QPF
view allData sourced from openFDA. This site is unofficial and independent of the FDA.