Clearance Summary
KODAK AMERLITE MAB FT3 ASSAY received FDA 510(k) clearance under submission number K922713, sponsored by Eastman Kodak Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1992-10-26.
- Submission: K922713
- Applicant / Sponsor: Eastman Kodak Company
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1695
- Decision date: 1992-10-26
Classification & Regulation
This clearance is catalogued under FDA product code CEC and 21 CFR 862.1695, within the Clinical Chemistry review panel as a Class II device.