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IL THYROXINE (T4) ASSAY SYSTEM

K903095 Class II Traditional
Decision Date
1990-08-23
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K903095
Product Code KLI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1990-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IL THYROXINE (T4) ASSAY SYSTEM received FDA 510(k) clearance under submission number K903095, sponsored by Instrumentation Laboratory CO. 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 1990-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code KLI and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.