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Nuheara IQbuds 2 PRO Hearing Aid

K221064 Class II Traditional
Decision Date
2022-10-30
Sponsor / Applicant
Nuheara Limited

Technical Specification

510(k) Submission ID K221064
Product Code QUH
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3325
Decision Date 2022-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nuheara IQbuds 2 PRO Hearing Aid received FDA 510(k) clearance under submission number K221064, sponsored by Nuheara Limited. 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 2022-10-30.

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.