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TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT

K900167 Class II Traditional
Decision Date
1990-01-22
Sponsor / Applicant
Behring Diagnostics, Inc.

Technical Specification

510(k) Submission ID K900167
Product Code DCF
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5040
Decision Date 1990-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TURBIQUANT IMMUNOGLOBULIN & ALBUMIN KIT received FDA 510(k) clearance under submission number K900167, sponsored by Behring Diagnostics, 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 1990-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code DCF and 21 CFR 866.5040, within the Immunology review panel as a Class II device.