meddevicedb.com FDA Device Reference

AUTO-TYMPANIGRAPH (TA-5A)

K811509 Class II Traditional
Decision Date
1981-06-16
Sponsor / Applicant
Teledyne Avionics Div. of Teledyne

Technical Specification

510(k) Submission ID K811509
Product Code ETY
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1090
Decision Date 1981-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO-TYMPANIGRAPH (TA-5A) received FDA 510(k) clearance under submission number K811509, 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 1981-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code ETY and 21 CFR 874.1090, within the Ear, Nose, Throat review panel as a Class II device.