meddevicedb.com FDA Device Reference

NOMAD TM-3400

K850109 Class II Traditional
Decision Date
1985-06-04
Sponsor / Applicant
Tracor Northern, Inc.

Technical Specification

510(k) Submission ID K850109
Product Code GWF
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1870
Decision Date 1985-06-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOMAD TM-3400 received FDA 510(k) clearance under submission number K850109, sponsored by Tracor Northern, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1985-06-04.

Classification & Regulation

This clearance is catalogued under FDA product code GWF and 21 CFR 882.1870, within the Neurology review panel as a Class II device.