Clearance Summary
ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROL received FDA 510(k) clearance under submission number K031607, sponsored by Orion Diagnostica, Div. Orion Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2003-10-10.
- Submission: K031607
- Applicant / Sponsor: Orion Diagnostica, Div. Orion Corp.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5270
- Decision date: 2003-10-10
Classification & Regulation
This clearance is catalogued under FDA product code DCK and 21 CFR 866.5270, within the Immunology review panel as a Class II device.