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TELESTAR I, HEARING AID

K860512 Class I Traditional
Decision Date
1986-03-17
Sponsor / Applicant
The Florida Hearing Aid Service

Technical Specification

510(k) Submission ID K860512
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1986-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TELESTAR I, HEARING AID received FDA 510(k) clearance under submission number K860512, sponsored by The Florida Hearing Aid Service. 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 1986-03-17.

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.