Clearance Summary
PARAGON CZE 2000 CAPILLARY ELECTROPHORESIS SYSTEM AND BUFFER-100 received FDA 510(k) clearance under submission number K002799, sponsored by Beckman Coulter, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2000-10-05.
- Submission: K002799
- Applicant / Sponsor: Beckman Coulter, Inc.
- Clearance pathway: Special
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5510
- Decision date: 2000-10-05
Classification & Regulation
This clearance is catalogued under FDA product code CFF and 21 CFR 866.5510, within the Immunology review panel as a Class II device.