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ETYMOTIC RESEARCH ER-10D OAE PROBE

K011114 Class II Traditional
Decision Date
2001-07-03
Sponsor / Applicant
Etymotic Research

Technical Specification

510(k) Submission ID K011114
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 2001-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ETYMOTIC RESEARCH ER-10D OAE PROBE received FDA 510(k) clearance under submission number K011114, 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 2001-07-03.

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.