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CIBA CORNING MAGIC LITE SQ SPECIFIC IGE ASSAY

K923420 Class II Traditional
Decision Date
1993-02-23
Sponsor / Applicant
Ciba Corning Diagnostics Corp.

Technical Specification

510(k) Submission ID K923420
Product Code DHB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5750
Decision Date 1993-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIBA CORNING MAGIC LITE SQ SPECIFIC IGE ASSAY received FDA 510(k) clearance under submission number K923420, 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 1993-02-23.

Classification & Regulation

This clearance is catalogued under FDA product code DHB and 21 CFR 866.5750, within the Immunology review panel as a Class II device.