Clearance Summary
FREELITE HUMAN LAMBDA FREE KIT received FDA 510(k) clearance under submission number K023131, sponsored by The Binding Site, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2003-01-21.
- Submission: K023131
- Applicant / Sponsor: The Binding Site, Ltd.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5550
- Decision date: 2003-01-21
Classification & Regulation
This clearance is catalogued under FDA product code DEH and 21 CFR 866.5550, within the Immunology review panel as a Class II device.