Clearance Summary
VARIANT II TURBO HBA1C KIT-2.0 VARIANT II TURBO HEMOGLOBIN TESTING SYSTEM received FDA 510(k) clearance under submission number K122472, sponsored by Bio-Rad Laboratories, Inc., Clinical Systems Divis. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2012-10-26.
- Submission: K122472
- Applicant / Sponsor: Bio-Rad Laboratories, Inc., Clinical Systems Divis
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7470
- Decision date: 2012-10-26
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.