Sonic Innovations Completely-In-The-Canal DSP Hearing Aid with Soft Shell

FDA 510(k) K984518 · Sonic Innovations, Inc.

Substantially Equivalent

510(k) numberK984518

Submission

Device name
Sonic Innovations Completely-In-The-Canal DSP Hearing Aid with Soft Shell
Applicant
Sonic Innovations, Inc.
Salt Lake City, UT, US
Received
December 21, 1998
Decision date
March 12, 1999
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.

Other 510(k)s with product code ESD

510(k)DeviceApplicantDecision
K232999Lyric4 Hearing AidESD · Traditional Sonova AG04/11/2024SE
K130790LYRIC2ESD · Traditional Phonak, LLC06/27/2013SE
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
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
K974152Opus 2 - Completely-In-Canal Series (Cic)ESD · Traditional Bernafon-Maico, Inc.12/15/1997SE

Questions and answers

When was Sonic Innovations Completely-In-The-Canal DSP Hearing Aid with Soft Shell cleared by the FDA?

Sonic Innovations Completely-In-The-Canal DSP Hearing Aid with Soft Shell (K984518) received a 510(k) decision of Substantially Equivalent on March 12, 1999, 81 days after the submission was received.

What is the product code of K984518?

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