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SYNCHRON LX SYSTEMS MICROALBUMIN CALIBRATOR

K000331 Class II Traditional
Decision Date
2000-02-10
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K000331
Product Code JIS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2000-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON LX SYSTEMS MICROALBUMIN CALIBRATOR received FDA 510(k) clearance under submission number K000331, 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 2000-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code JIS and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.