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HEARING CHECKER(TM), DESKTOP MODEL

K904622 Class II Traditional
Decision Date
1991-09-17
Sponsor / Applicant
Qualitone Hearing Aids and Audiometers

Technical Specification

510(k) Submission ID K904622
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 1991-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARING CHECKER(TM), DESKTOP MODEL received FDA 510(k) clearance under submission number K904622, sponsored by Qualitone Hearing Aids and Audiometers. 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 1991-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code EWO and 21 CFR 874.1050, within the Ear, Nose, Throat review panel as a Class II device.