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PHONIC EAR, PE 860C, PE 860PPC AND PE 860 PPCL

K874304 Class I Traditional
Decision Date
1987-11-20
Sponsor / Applicant
Phonic Ear, Inc.

Technical Specification

510(k) Submission ID K874304
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1987-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHONIC EAR, PE 860C, PE 860PPC AND PE 860 PPCL received FDA 510(k) clearance under submission number K874304, 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 1987-11-20.

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.