meddevicedb.com FDA Device Reference

MODEL CA, HEARING AID

K862095 Class I Traditional
Decision Date
1986-06-26
Sponsor / Applicant
Fine-Tune

Technical Specification

510(k) Submission ID K862095
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1986-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL CA, HEARING AID received FDA 510(k) clearance under submission number K862095, sponsored by Fine-Tune. 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 1986-06-26.

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.