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SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT

K974050 Class II Traditional
Decision Date
1997-11-24
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K974050
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 1997-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT received FDA 510(k) clearance under submission number K974050, sponsored by Beckman Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1997-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code DCK and 21 CFR 866.5270, within the Immunology review panel as a Class II device.