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SYNCHRON CX5CE CLINICAL ANALYZER

K926060 Class I Traditional
Decision Date
1993-02-12
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K926060
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 1993-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON CX5CE CLINICAL ANALYZER received FDA 510(k) clearance under submission number K926060, sponsored by Beckman Instruments, 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 1993-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.