meddevicedb.com FDA Device Reference

TEOAE25

K030016 Class II Traditional
Decision Date
2003-03-28
Sponsor / Applicant
Interacoustics A/S, Assens

Technical Specification

510(k) Submission ID K030016
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 2003-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEOAE25 received FDA 510(k) clearance under submission number K030016, sponsored by Interacoustics A/S, Assens. 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 2003-03-28.

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.