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QUANTIA BETA-2 MICROGLOBULIN, MODEL: 302822307

K072078 Class II Traditional
Decision Date
2007-12-19
Sponsor / Applicant
Biokit, S.A.

Technical Specification

510(k) Submission ID K072078
Product Code JZG
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5630
Decision Date 2007-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTIA BETA-2 MICROGLOBULIN, MODEL: 302822307 received FDA 510(k) clearance under submission number K072078, sponsored by Biokit, S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2007-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code JZG and 21 CFR 866.5630, within the Immunology review panel as a Class II device.