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MODIFICATION TO: REAADS ANTI-PHOSPHATIDYLSERINE IGG/IGM SEMI-QUANTITATIVE TEST KIT

K012567 Class II Special
Decision Date
2001-08-23
Sponsor / Applicant
Corgenix, Inc.

Technical Specification

510(k) Submission ID K012567
Product Code MID
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5660
Decision Date 2001-08-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: REAADS ANTI-PHOSPHATIDYLSERINE IGG/IGM SEMI-QUANTITATIVE TEST KIT received FDA 510(k) clearance under submission number K012567, 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 2001-08-23.

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.