Model Alpha Behind-The-Ear Hearing Instrument

FDA 510(k) K962228 · Ototech Intl., Inc.

Substantially Equivalent

510(k) numberK962228

Submission

Device name
Model Alpha Behind-The-Ear Hearing Instrument
Applicant
Ototech Intl., Inc.
Oklahoma City, OK, US
Received
June 10, 1996
Decision date
August 28, 1996
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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K081136Lyric Hearing AidESD · Traditional Insound Medical, Inc.05/08/2008SE
K021867Insound XT Series Hearing AidESD · Traditional Insound Medical, Inc.11/19/2002SE
K003558Tci Combi (Tinnitus Control Instrument Combination)ESD · Traditional Siemens Hearing Instruments, Inc.04/24/2001SE
K984518Sonic Innovations Completely-In-The-Canal DSP Hearing Aid with Soft ShellESD · Traditional Sonic Innovations, Inc.03/12/1999SE
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
K974211Opus 2 - Full Concha Series - IteESD · Traditional Bernafon-Maico, Inc.12/15/1997SE

Questions and answers

When was Model Alpha Behind-The-Ear Hearing Instrument cleared by the FDA?

Model Alpha Behind-The-Ear Hearing Instrument (K962228) received a 510(k) decision of Substantially Equivalent on August 28, 1996, 79 days after the submission was received.

What is the product code of K962228?

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