meddevicedb.com FDA Device Reference

MULTIFOCUS COMPACT BTE HEARING AID

K933307 Class I Traditional
Decision Date
1993-08-23
Sponsor / Applicant
Oticon, Inc.

Technical Specification

510(k) Submission ID K933307
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1993-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIFOCUS COMPACT BTE HEARING AID received FDA 510(k) clearance under submission number K933307, sponsored by Oticon, 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 1993-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code ESD and 21 CFR 874.3300, within the Ear, Nose, Throat review panel as a Class I device.