Bose Hearing Aid— 510(k) DEN180026

Unknown

Bose Corporation

FDA 510(k) clearance DEN180026 for Bose Hearing Aid, Unknown on 2018-10-05. Applicant: Bose Corporation. Device class: 2.

Clearance details

Applicant: Bose Corporation
Product code: Code QDD
Device class: Class 2
Regulation: 21 CFR 874.3325
Advisory panel: Ear, Nose, Throat
Date received: 2018-05-11
Decision date: 2018-10-05
Decision: Unknown
Clearance type: Direct
Location: Framingham, MA, US

View on FDA.gov ↗

Recent devices under product code QDD

K223911 — Lumen 155-SF2023-10-17
K220403 — Vibe SF Self-Fitting Hearing Aid2022-08-12
K220303 — MDHearingAid app, MDHearingAid Smart hearing aids2022-08-04
K213424 — Jabra Enhance Plus2022-01-19
K212609 — BHA100 Series Braun Clear Hearing Aid2022-01-05

More clearances from Bose Corporation

K211008 — Bose SoundControl Hearing Aids2021-05-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.