meddevicedb.com FDA Device Reference

CIBA CORNING MAGIC LITE FERRITIN

K873573 Class II Traditional
Decision Date
1987-10-07
Sponsor / Applicant
Ciba Corning Diagnostics Corp.

Technical Specification

510(k) Submission ID K873573
Product Code DBF
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5340
Decision Date 1987-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIBA CORNING MAGIC LITE FERRITIN received FDA 510(k) clearance under submission number K873573, sponsored by Ciba Corning Diagnostics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1987-10-07.

Classification & Regulation

This clearance is catalogued under FDA product code DBF and 21 CFR 866.5340, within the Immunology review panel as a Class II device.