Clearance Summary
ALERE CHOLESTECH LDX ANALYZER, ALERE CHOLESTECH LDX LIPID PROFILE - GLU CASSETTE received FDA 510(k) clearance under submission number K120615, sponsored by Alere San Diego Inc. Dba Biosite,Innovacon,Hemosen. 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 2013-05-15.
- Submission: K120615
- Applicant / Sponsor: Alere San Diego Inc. Dba Biosite,Innovacon,Hemosen
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1345
- Decision date: 2013-05-15
Classification & Regulation
This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.