meddevicedb.com FDA Device Reference

AGGLUTINATION TEST FOR TOTAL IGE

K843369 Class II Traditional
Decision Date
1984-11-14
Sponsor / Applicant
Scientific Research

Technical Specification

510(k) Submission ID K843369
Product Code DGC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1984-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AGGLUTINATION TEST FOR TOTAL IGE received FDA 510(k) clearance under submission number K843369, sponsored by Scientific Research. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1984-11-14.

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.