meddevicedb.com FDA Device Reference

SMART COUPLER, MODEL M015401

K073384 Class II Traditional
Decision Date
2008-02-28
Sponsor / Applicant
Intelligent Hearing Systems

Technical Specification

510(k) Submission ID K073384
Product Code GWJ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1900
Decision Date 2008-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMART COUPLER, MODEL M015401 received FDA 510(k) clearance under submission number K073384, sponsored by Intelligent Hearing Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2008-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code GWJ and 21 CFR 882.1900, within the Neurology review panel as a Class II device.