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AU BICARBONATE REAGENT

K131546 Class II Traditional
Decision Date
2013-10-09
Sponsor / Applicant
Beckman Coulter Ireland, Inc.

Technical Specification

510(k) Submission ID K131546
Product Code KHS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1160
Decision Date 2013-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AU BICARBONATE REAGENT received FDA 510(k) clearance under submission number K131546, sponsored by Beckman Coulter Ireland, 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 2013-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code KHS and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.