meddevicedb.com FDA Device Reference

Self-Fitting hearing aids

K221052 Class II Traditional
Decision Date
2023-09-25
Sponsor / Applicant
Huizhou Jinghao Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K221052
Product Code QUH
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3325
Decision Date 2023-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Self-Fitting hearing aids received FDA 510(k) clearance under submission number K221052, sponsored by Huizhou Jinghao Medical Technology Co., Ltd.. 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 2023-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code QUH and 21 CFR 874.3325, within the Ear, Nose, Throat review panel as a Class II device.