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CUB DIS OTOACOUSTIC EMISSIONS TEST INSTRUMENT

K930553 Class II Traditional
Decision Date
1993-09-29
Sponsor / Applicant
Etymotic Research

Technical Specification

510(k) Submission ID K930553
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 1993-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CUB DIS OTOACOUSTIC EMISSIONS TEST INSTRUMENT received FDA 510(k) clearance under submission number K930553, sponsored by Etymotic Research. 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 1993-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code EWO and 21 CFR 874.1050, within the Ear, Nose, Throat review panel as a Class II device.