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IMAGE-IGE

K853025 Class II Traditional
Decision Date
1985-08-22
Sponsor / Applicant
Clinical Reference Laboratory, Inc.

Technical Specification

510(k) Submission ID K853025
Product Code DGC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1985-08-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGE-IGE received FDA 510(k) clearance under submission number K853025, sponsored by Clinical Reference Laboratory, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1985-08-22.

Classification & Regulation

This clearance is catalogued under FDA product code DGC and 21 CFR 866.5510, within the Immunology review panel as a Class II device.