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SEARS BEHIND-THE-EAR HEARING AID

K800113 Class I Traditional
Decision Date
1980-02-11
Sponsor / Applicant
Int'L Hearing Aids, Inc.

Technical Specification

510(k) Submission ID K800113
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1980-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SEARS BEHIND-THE-EAR HEARING AID received FDA 510(k) clearance under submission number K800113, sponsored by Int'L Hearing Aids, 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 1980-02-11.

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.