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HEARING AIDS (MODEL E-552 S-712)

K761216 Class I Traditional
Decision Date
1976-12-16
Sponsor / Applicant
Vicon Instrument Co.

Technical Specification

510(k) Submission ID K761216
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1976-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARING AIDS (MODEL E-552 S-712) received FDA 510(k) clearance under submission number K761216, sponsored by Vicon Instrument Co.. 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 1976-12-16.

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.