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LINICAL PROTEIN III CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN SYSTEM

K953926 Class II Traditional
Decision Date
1995-09-15
Sponsor / Applicant
International Enzymes, Inc.

Technical Specification

510(k) Submission ID K953926
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 1995-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LINICAL PROTEIN III CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN SYSTEM received FDA 510(k) clearance under submission number K953926, sponsored by International Enzymes, 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 1995-09-15.

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.