meddevicedb.com FDA Device Reference

ALLERGENTICS TOTAL IGE/THEOPHYLLINE

K842970 Class I Traditional
Decision Date
1984-08-29
Sponsor / Applicant
Allergenetics

Technical Specification

510(k) Submission ID K842970
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1984-08-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALLERGENTICS TOTAL IGE/THEOPHYLLINE received FDA 510(k) clearance under submission number K842970, sponsored by Allergenetics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1984-08-29.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.