510(k) K241456
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 7, 2025
- Date Received
- May 22, 2024
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Genetic Variant Detection And Health Risk Assessment System
- Device Class
- Class II
- Regulation Number
- 866.5950
- Review Panel
- IM
- Submission Type
A qualitative in vitro molecular test that detects variants in genomic DNA isolated from human specimens. This assessment system provides users with a genetic health risk assessment of developing a disease and is intended to inform users of lifestyle choices and/or encourage conversations with a healthcare professional. This assessment system is for over-the-counter use. This device does not determine the persons overall risk of developing a disease.