Clearance Summary
LEECO T3% DIAGNOSTIC KIT received FDA 510(k) clearance under submission number K822575, sponsored by Leeco Diagnostics, Inc.. 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 1982-09-30.
- Submission: K822575
- Applicant / Sponsor: Leeco Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1715
- Decision date: 1982-09-30
Classification & Regulation
This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.