meddevicedb.com FDA Device Reference

HEARING AID (ALL-IN-THE-EAR)

K912399 Class I Traditional
Decision Date
1992-03-12
Sponsor / Applicant
Carlson'S Heritage Hearing Aid Center

Technical Specification

510(k) Submission ID K912399
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1992-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARING AID (ALL-IN-THE-EAR) received FDA 510(k) clearance under submission number K912399, sponsored by Carlson'S Heritage Hearing Aid Center. 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 1992-03-12.

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.