Clearance Summary
LEECO PROGESTERONE-QUANT DIAGNOSTIC TEST KIT received FDA 510(k) clearance under submission number K850056, 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 1985-02-06.
- Submission: K850056
- Applicant / Sponsor: Leeco Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1620
- Decision date: 1985-02-06
Classification & Regulation
This clearance is catalogued under FDA product code JLS and 21 CFR 862.1620, within the Clinical Chemistry review panel as a Class I device.