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SYNCHRON LX SYSTEMS COMPLEMENT C3 (C3) REAGENT, SYNCHRON LX SYSTEMS COMPLEMENT C4 (C4) REAGENT, SYNCHRON LX SYSTEMS CALI

K032035 Class II Traditional
Decision Date
2003-08-07
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K032035
Product Code CZW
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5240
Decision Date 2003-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON LX SYSTEMS COMPLEMENT C3 (C3) REAGENT, SYNCHRON LX SYSTEMS COMPLEMENT C4 (C4) REAGENT, SYNCHRON LX SYSTEMS CALI received FDA 510(k) clearance under submission number K032035, sponsored by Beckman Coulter, 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 2003-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code CZW and 21 CFR 866.5240, within the Immunology review panel as a Class II device.