meddevicedb.com FDA Device Reference

CLINICAL AUDIOMETER MODEL TA-200

K801325 Class II Traditional
Decision Date
1980-06-30
Sponsor / Applicant
Teledyne Avionics Div. of Teledyne

Technical Specification

510(k) Submission ID K801325
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 1980-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLINICAL AUDIOMETER MODEL TA-200 received FDA 510(k) clearance under submission number K801325, sponsored by Teledyne Avionics Div. of Teledyne. 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 1980-06-30.

Classification & Regulation

This clearance is catalogued under FDA product code EWO and 21 CFR 874.1050, within the Ear, Nose, Throat review panel as a Class II device.