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UBI MAGIWEL TRIIODOTHYRONINE(T3) QUANTITATIVE

K961236 Class II Traditional
Decision Date
1996-05-30
Sponsor / Applicant
United Biotech, Inc.

Technical Specification

510(k) Submission ID K961236
Product Code CDP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1710
Decision Date 1996-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UBI MAGIWEL TRIIODOTHYRONINE(T3) QUANTITATIVE received FDA 510(k) clearance under submission number K961236, sponsored by United Biotech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1996-05-30.

Classification & Regulation

This clearance is catalogued under FDA product code CDP and 21 CFR 862.1710, within the Clinical Chemistry review panel as a Class II device.