meddevicedb.com FDA Device Reference

HEARING AID, UNITRON MODEL UM60

K870503 Class I Traditional
Decision Date
1987-03-11
Sponsor / Applicant
Unitron Industries, Inc.

Technical Specification

510(k) Submission ID K870503
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1987-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARING AID, UNITRON MODEL UM60 received FDA 510(k) clearance under submission number K870503, sponsored by Unitron Industries, 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 1987-03-11.

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.