meddevicedb.com FDA Device Reference

HEARING-AID

K872552 Class I Traditional
Decision Date
1987-08-03
Sponsor / Applicant
Audio-Technica U.S., Inc.

Technical Specification

510(k) Submission ID K872552
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1987-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARING-AID received FDA 510(k) clearance under submission number K872552, sponsored by Audio-Technica U.S., 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 1987-08-03.

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.