meddevicedb.com FDA Device Reference

Natus Quantum

K143440 Class II Traditional
Decision Date
2015-04-20
Sponsor / Applicant
Natus Medical Incorporated

Technical Specification

510(k) Submission ID K143440
Product Code GWQ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 2015-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Natus Quantum received FDA 510(k) clearance under submission number K143440, sponsored by Natus Medical Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2015-04-20.

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.