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iQ200 System, iChemVELOCITY Automated Urine Chemistry System

K210127 Class II Traditional
Decision Date
2021-07-02
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K210127
Product Code LKM
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5200
Decision Date 2021-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

iQ200 System, iChemVELOCITY Automated Urine Chemistry System received FDA 510(k) clearance under submission number K210127, sponsored by Beckman Coulter, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2021-07-02.

Classification & Regulation

This clearance is catalogued under FDA product code LKM and 21 CFR 864.5200, within the Hematology review panel as a Class II device.