meddevicedb.com FDA Device Reference

BRAHMS DIAGNOSTICA LUMITEST TRAK HUMAN

K033454 Class II Traditional
Decision Date
2004-03-22
Sponsor / Applicant
Brahms Diagnostica, LLC

Technical Specification

510(k) Submission ID K033454
Product Code JZO
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5870
Decision Date 2004-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRAHMS DIAGNOSTICA LUMITEST TRAK HUMAN received FDA 510(k) clearance under submission number K033454, sponsored by Brahms Diagnostica, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2004-03-22.

Classification & Regulation

This clearance is catalogued under FDA product code JZO and 21 CFR 866.5870, within the Immunology review panel as a Class II device.