meddevicedb.com FDA Device Reference

TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)

K003558 Class I Traditional
Decision Date
2001-04-24
Sponsor / Applicant
Siemens Hearing Instruments, Inc.

Technical Specification

510(k) Submission ID K003558
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 2001-04-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION) received FDA 510(k) clearance under submission number K003558, sponsored by Siemens Hearing Instruments, 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 2001-04-24.

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.