Clearance Summary
RETINOL BINDING RID KIT received FDA 510(k) clearance under submission number K955881, 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 1996-03-22.
- Submission: K955881
- Applicant / Sponsor: The Binding Site, Ltd.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class I
- Regulation citation: 21 CFR 866.5765
- Decision date: 1996-03-22
Classification & Regulation
This clearance is catalogued under FDA product code CZS and 21 CFR 866.5765, within the Immunology review panel as a Class I device.