Clearance Summary
Lumipulse G pTau217/ß-Amyloid 1-42 Plasma Ratio received FDA 510(k) clearance under submission number K242706, sponsored by Fujirebio Diagnostics,Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2025-05-16.
- Submission: K242706
- Applicant / Sponsor: Fujirebio Diagnostics,Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5840
- Decision date: 2025-05-16
Classification & Regulation
This clearance is catalogued under FDA product code SET and 21 CFR 866.5840, within the Immunology review panel as a Class II device.