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IL TEST IMMUNOGLOBULIN A

K920014 Class II Traditional
Decision Date
1992-06-16
Sponsor / Applicant
Instrumentation Laboratory CO

Technical Specification

510(k) Submission ID K920014
Product Code CZP
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1992-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IL TEST IMMUNOGLOBULIN A received FDA 510(k) clearance under submission number K920014, sponsored by Instrumentation Laboratory CO. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1992-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code CZP and 21 CFR 866.5510, within the Immunology review panel as a Class II device.