meddevicedb.com FDA Device Reference

HEARING AID CUSTOM ITE

K813206 Class I Traditional
Decision Date
1981-12-08
Sponsor / Applicant
Duvan Acoustics, Inc.

Technical Specification

510(k) Submission ID K813206
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1981-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARING AID CUSTOM ITE received FDA 510(k) clearance under submission number K813206, sponsored by Duvan Acoustics, 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 1981-12-08.

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.