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AUTOSTAT II ANTI-CARDIOLIPIN IGG ELISA

K992440 Class II Traditional
Decision Date
1999-09-21
Sponsor / Applicant
Cogent Diagnotics , Ltd.

Technical Specification

510(k) Submission ID K992440
Product Code MID
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5660
Decision Date 1999-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOSTAT II ANTI-CARDIOLIPIN IGG ELISA received FDA 510(k) clearance under submission number K992440, sponsored by Cogent Diagnotics , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1999-09-21.

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.