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AUDITORY STIMULATOR

K813557 Class II Traditional
Decision Date
1982-01-19
Sponsor / Applicant
Western Advanced Technology, Inc.

Technical Specification

510(k) Submission ID K813557
Product Code ETS
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1120
Decision Date 1982-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUDITORY STIMULATOR received FDA 510(k) clearance under submission number K813557, sponsored by Western Advanced Technology, 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 1982-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code ETS and 21 CFR 874.1120, within the Ear, Nose, Throat review panel as a Class II device.