Clearance Summary
LASER CERULOPLASMIN KIT(CERULOPLASMIN REAGENTS) received FDA 510(k) clearance under submission number K852247, sponsored by Behring Diagnostics, 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 1985-07-10.
- Submission: K852247
- Applicant / Sponsor: Behring Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5210
- Decision date: 1985-07-10
Classification & Regulation
This clearance is catalogued under FDA product code DDB and 21 CFR 866.5210, within the Immunology review panel as a Class II device.