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Sound Options Tinnitus Treatment

K161562 Class II Traditional
Decision Date
2016-09-28
Sponsor / Applicant
Sound Options Tinnitus Treatments, Inc.

Technical Specification

510(k) Submission ID K161562
Product Code KLW
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3400
Decision Date 2016-09-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sound Options Tinnitus Treatment received FDA 510(k) clearance under submission number K161562, sponsored by Sound Options Tinnitus Treatments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2016-09-28.

Classification & Regulation

This clearance is catalogued under FDA product code KLW and 21 CFR 874.3400, within the Ear, Nose, Throat review panel as a Class II device.