Clearance Summary
LEUKO EZ VUE received FDA 510(k) clearance under submission number K071712, sponsored by Techlab Inc., Corporate Research Center. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2007-12-04.
- Submission: K071712
- Applicant / Sponsor: Techlab Inc., Corporate Research Center
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class I
- Regulation citation: 21 CFR 866.5570
- Decision date: 2007-12-04
Classification & Regulation
This clearance is catalogued under FDA product code DEG and 21 CFR 866.5570, within the Immunology review panel as a Class I device.