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SYNCHRON SYSTEMS HDL CHOLESTEROL (HDLD) REAGENT

K040767 Class I Traditional
Decision Date
2004-06-07
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K040767
Product Code LBS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 2004-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON SYSTEMS HDL CHOLESTEROL (HDLD) REAGENT received FDA 510(k) clearance under submission number K040767, sponsored by Beckman Coulter, Inc.. 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 2004-06-07.

Classification & Regulation

This clearance is catalogued under FDA product code LBS and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.