Clearance Summary
IGD DIAGNOSTIC TEST KITS received FDA 510(k) clearance under submission number K051299, 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 2005-11-23.
- Submission: K051299
- Applicant / Sponsor: The Binding Site, Ltd.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5510
- Decision date: 2005-11-23
Classification & Regulation
This clearance is catalogued under FDA product code CZJ and 21 CFR 866.5510, within the Immunology review panel as a Class II device.