meddevicedb.com FDA Device Reference

UBI MAGIWEL(TM) ANA QUANTITATIVE

K910033 Class II Traditional
Decision Date
1991-01-25
Sponsor / Applicant
United Biotech, Inc.

Technical Specification

510(k) Submission ID K910033
Product Code LJM
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1991-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UBI MAGIWEL(TM) ANA QUANTITATIVE received FDA 510(k) clearance under submission number K910033, sponsored by United Biotech, 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 1991-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code LJM and 21 CFR 866.5100, within the Immunology review panel as a Class II device.