Clearance Summary
BAYER LIGAND PLUS 1, 2, 3 CONTROLS received FDA 510(k) clearance under submission number K030452, sponsored by Bayer Diagnostics Corp.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2003-03-03.
- Submission: K030452
- Applicant / Sponsor: Bayer Diagnostics Corp.
- Clearance pathway: Abbreviated
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1660
- Decision date: 2003-03-03
Classification & Regulation
This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.