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BECKMAN IMMUNOGLOBULIN G (IGG) REAGENT, URINE APPLICATION, URINE PROTEIN CALIBRATOR, CONTROL

K951635 Class II Traditional
Decision Date
1995-05-15
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K951635
Product Code DEW
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1995-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BECKMAN IMMUNOGLOBULIN G (IGG) REAGENT, URINE APPLICATION, URINE PROTEIN CALIBRATOR, CONTROL received FDA 510(k) clearance under submission number K951635, 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 1995-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code DEW and 21 CFR 866.5510, within the Immunology review panel as a Class II device.