Clearance Summary
ABBOTT RF EIA DIAGNOSTIC KIT received FDA 510(k) clearance under submission number K850373, sponsored by Abbott Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1985-03-01.
- Submission: K850373
- Applicant / Sponsor: Abbott Laboratories
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5775
- Decision date: 1985-03-01
Classification & Regulation
This clearance is catalogued under FDA product code DHR and 21 CFR 866.5775, within the Immunology review panel as a Class II device.