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ALLERG-E IGE ENZYME IMMUNOASSAY KIT

K853607 Class II Traditional
Decision Date
1985-11-07
Sponsor / Applicant
Dexall Biomedical Labs, Inc.

Technical Specification

510(k) Submission ID K853607
Product Code DGO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1985-11-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALLERG-E IGE ENZYME IMMUNOASSAY KIT received FDA 510(k) clearance under submission number K853607, sponsored by Dexall Biomedical Labs, 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 1985-11-07.

Classification & Regulation

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