Clearance Summary
LEECO GLYCO-HEMOGLOBIN DIAG. TEST KIT received FDA 510(k) clearance under submission number K801289, sponsored by Leeco Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1980-06-30.
- Submission: K801289
- Applicant / Sponsor: Leeco Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7470
- Decision date: 1980-06-30
Classification & Regulation
This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.