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TOTAL PROTEIN REAGENT BECKMAN SYNCHRON CX3 ANALYZE

K913978 Class II Traditional
Decision Date
1991-10-09
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K913978
Product Code CEK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1635
Decision Date 1991-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL PROTEIN REAGENT BECKMAN SYNCHRON CX3 ANALYZE received FDA 510(k) clearance under submission number K913978, 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 1991-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code CEK and 21 CFR 862.1635, within the Clinical Chemistry review panel as a Class II device.