Clearance Summary
KRONUS GAD AUTOANTIBODY ELISA ASSAY KIT received FDA 510(k) clearance under submission number K072135, sponsored by Kronus Market Development Associates, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2007-11-07.
- Submission: K072135
- Applicant / Sponsor: Kronus Market Development Associates, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5660
- Decision date: 2007-11-07
Classification & Regulation
This clearance is catalogued under FDA product code NWG and 21 CFR 866.5660, within the Immunology review panel as a Class II device.