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MDHearingAid app, MDHearingAid Smart hearing aids

K220303 Class II Traditional
Decision Date
2022-08-04
Sponsor / Applicant
Mdhearingaid

Technical Specification

510(k) Submission ID K220303
Product Code QDD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3325
Decision Date 2022-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MDHearingAid app, MDHearingAid Smart hearing aids received FDA 510(k) clearance under submission number K220303, sponsored by Mdhearingaid. 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 2022-08-04.

Classification & Regulation

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