meddevicedb.com FDA Device Reference

Hearing Healthcare Pro

K183201 Class II Traditional
Decision Date
2019-03-06
Sponsor / Applicant
Db Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K183201
Product Code ETY
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1090
Decision Date 2019-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hearing Healthcare Pro received FDA 510(k) clearance under submission number K183201, sponsored by Db Diagnostic Systems, 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 2019-03-06.

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.