meddevicedb.com FDA Device Reference

IMMUNOGLOBULIN E TEST KIT

K800995 Class II Traditional
Decision Date
1980-05-14
Sponsor / Applicant
Calbiochem-Behring Corp.

Technical Specification

510(k) Submission ID K800995
Product Code DGO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1980-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMUNOGLOBULIN E TEST KIT received FDA 510(k) clearance under submission number K800995, sponsored by Calbiochem-Behring 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 1980-05-14.

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.