Model C-1 Hearing Aid

FDA 510(k) K973043 · Better Hearing, Inc.

Substantially Equivalent

510(k) numberK973043

Submission

Device name
Model C-1 Hearing Aid
Applicant
Better Hearing, Inc.
Herndon, VA, US
Received
August 15, 1997
Decision date
October 27, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ESD – Hearing Aid, Air-Conduction, Prescription
Device class
Class I (low risk)
Regulation
21 CFR 874.3300
Specialty
Ear, Nose, Throat

An air-conduction hearing aid is a wearable sound amplifying device intended to compensate for impaired hearing that conducts sound to the ear through the air. This is a prescription hearing aid.

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K974751Tranquil Tri-Oe, Tranquil Tri-Coe, Tranquil Tri-CicESD · Traditional General Hearing Instruments, Inc.03/06/1998SE
K974242Argosy Programmable OnqueESD · Traditional Argosy Electronics01/20/1998SE
K973880Sonix Hearing Aid Fitting and Programming SystemESD · Traditional Sonix Technologies, Inc.01/12/1998SE
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More from Bernafon-Maico, Inc.

510(k)DeviceDecision
K971298Better Hearing, Inc. Model L-1 Hearing AidESD · Traditional 07/23/1997SE

Questions and answers

When was Model C-1 Hearing Aid cleared by the FDA?

Model C-1 Hearing Aid (K973043) received a 510(k) decision of Substantially Equivalent on October 27, 1997, 73 days after the submission was received.

What is the product code of K973043?

The FDA product code is ESD – Hearing Aid, Air-Conduction, Prescription, a Class I (low risk) device regulated under 21 CFR 874.3300.