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REAADS II ANTI-CARDIOLIPIN IGG SEMI-QUANTITATIVE TEST KIT, MODEL 11139

K032868 Class II Special
Decision Date
2003-10-14
Sponsor / Applicant
Corgenix, Inc.

Technical Specification

510(k) Submission ID K032868
Product Code MID
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5660
Decision Date 2003-10-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAADS II ANTI-CARDIOLIPIN IGG SEMI-QUANTITATIVE TEST KIT, MODEL 11139 received FDA 510(k) clearance under submission number K032868, sponsored by Corgenix, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2003-10-14.

Classification & Regulation

This clearance is catalogued under FDA product code MID and 21 CFR 866.5660, within the Immunology review panel as a Class II device.