meddevicedb.com FDA Device Reference

BIO-LOGIC INSERT EARPHONES

K031352 Class II Traditional
Decision Date
2003-07-16
Sponsor / Applicant
Bio-Logic Systems Corp.

Technical Specification

510(k) Submission ID K031352
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 2003-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-LOGIC INSERT EARPHONES received FDA 510(k) clearance under submission number K031352, sponsored by Bio-Logic Systems Corp.. 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 2003-07-16.

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.