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MODEL TM5 BEHIND EAR TINNITUS MASKER

K791790 Class II Traditional
Decision Date
1979-10-26
Sponsor / Applicant
Starkey Laboratories, Inc.

Technical Specification

510(k) Submission ID K791790
Product Code KLW
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3400
Decision Date 1979-10-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL TM5 BEHIND EAR TINNITUS MASKER received FDA 510(k) clearance under submission number K791790, sponsored by Starkey Laboratories, 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 1979-10-26.

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.