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Dr.MUSIC 3s

K172451 Class II Traditional
Decision Date
2017-11-17
Sponsor / Applicant
Smartmedicaldevice Co., Ltd.

Technical Specification

510(k) Submission ID K172451
Product Code NUH
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2017-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dr.MUSIC 3s received FDA 510(k) clearance under submission number K172451, sponsored by Smartmedicaldevice Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2017-11-17.

Classification & Regulation

This clearance is catalogued under FDA product code NUH and 21 CFR 882.5890, within the Neurology review panel as a Class II device.