meddevicedb.com FDA Device Reference

MODEL 339 TELECROS WIRELESS BICROS

K792462 Class I Traditional
Decision Date
1980-01-09
Sponsor / Applicant
Telex Communications, Inc.

Technical Specification

510(k) Submission ID K792462
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1980-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 339 TELECROS WIRELESS BICROS received FDA 510(k) clearance under submission number K792462, sponsored by Telex Communications, Inc.. 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 1980-01-09.

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.