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SONOTONE BEHIND THE EAR MODEL ST 47I

K914898 Class I Traditional
Decision Date
1992-01-09
Sponsor / Applicant
Sonotone Hearing Instruments

Technical Specification

510(k) Submission ID K914898
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1992-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONOTONE BEHIND THE EAR MODEL ST 47I received FDA 510(k) clearance under submission number K914898, sponsored by Sonotone Hearing Instruments. 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 1992-01-09.

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.