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XLTEK EMU40EX EEG Headbox

K163163 Class II Special
Decision Date
2016-12-14
Sponsor / Applicant
Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)

Technical Specification

510(k) Submission ID K163163
Product Code GWQ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 2016-12-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XLTEK EMU40EX EEG Headbox received FDA 510(k) clearance under submission number K163163, sponsored by Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek). The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2016-12-14.

Classification & Regulation

This clearance is catalogued under FDA product code GWQ and 21 CFR 882.1400, within the Neurology review panel as a Class II device.