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IN-THE-EAR-CANAL HEARING AID

K842980 Class I Traditional
Decision Date
1984-09-05
Sponsor / Applicant
Ear Care Hearing Systems, Inc.

Technical Specification

510(k) Submission ID K842980
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1984-09-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IN-THE-EAR-CANAL HEARING AID received FDA 510(k) clearance under submission number K842980, sponsored by Ear Care Hearing Systems, 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 1984-09-05.

Classification & Regulation

This clearance is catalogued under FDA product code ESD and 21 CFR 874.3300, within the Ear, Nose, Throat review panel as a Class I device.