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GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)

K950730 Class II Traditional
Decision Date
1995-06-30
Sponsor / Applicant
Phonic Ear, Inc.

Technical Specification

510(k) Submission ID K950730
Product Code EPF
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3320
Decision Date 1995-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM) received FDA 510(k) clearance under submission number K950730, sponsored by Phonic Ear, 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 1995-06-30.

Classification & Regulation

This clearance is catalogued under FDA product code EPF and 21 CFR 874.3320, within the Ear, Nose, Throat review panel as a Class II device.