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UNICEL DXC SYNCHRON SYSTEMS GLUCOSE REAGENT (GLUH)

K131189 Class II Traditional
Decision Date
2014-04-17
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K131189
Product Code CFR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2014-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNICEL DXC SYNCHRON SYSTEMS GLUCOSE REAGENT (GLUH) received FDA 510(k) clearance under submission number K131189, 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 2014-04-17.

Classification & Regulation

This clearance is catalogued under FDA product code CFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.