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PHONIC EAR

K940313 Class II Traditional
Decision Date
1994-03-22
Sponsor / Applicant
Phonic Ear, Inc.

Technical Specification

510(k) Submission ID K940313
Product Code EPF
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3320
Decision Date 1994-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHONIC EAR received FDA 510(k) clearance under submission number K940313, 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 1994-03-22.

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.