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BECKMAN ALPHA-1-MICROGLOBULIN (A1M) REAGENT

K933078 Class I Traditional
Decision Date
1994-01-11
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K933078
Product Code MGA
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5400
Decision Date 1994-01-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BECKMAN ALPHA-1-MICROGLOBULIN (A1M) REAGENT received FDA 510(k) clearance under submission number K933078, 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 1994-01-11.

Classification & Regulation

This clearance is catalogued under FDA product code MGA and 21 CFR 866.5400, within the Immunology review panel as a Class I device.