meddevicedb.com FDA Device Reference

X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE

K131383 Class II Traditional
Decision Date
2013-11-27
Sponsor / Applicant
Advanced Brain Monitoring, Inc.

Technical Specification

510(k) Submission ID K131383
Product Code GWQ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 2013-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE received FDA 510(k) clearance under submission number K131383, sponsored by Advanced Brain Monitoring, 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 2013-11-27.

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.