← Product Code [ESD](/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ESD) · K964508

# UNITRON MODEL ICON AOHP +4 (ICON AOHP +4) (K964508)

_Unitron Industries, Inc. · ESD · Nov 27, 1996 · Ear, Nose, Throat · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ESD/K964508

## Device Facts

- **Applicant:** Unitron Industries, Inc.
- **Product Code:** [ESD](/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ESD.md)
- **Decision Date:** Nov 27, 1996
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 874.3300
- **Device Class:** Class 1
- **Review Panel:** Ear, Nose, Throat
- **Attributes:** Therapeutic

## Intended Use

To amplify and transmit sound via air conduction to the ear.

## Device Story

Behind-the-ear (BTE) hearing aid; amplifies and transmits sound via air conduction. Features four fitter controls (power, compression limiting, active low cut tone, high cut tone); Class D circuitry for battery efficiency; telecoil with preamplifier. User-operated volume control and microphone/telecoil/off switch. Powered by size 13 battery. Assembled from standard industry components. Used by patients to improve hearing.

## Clinical Evidence

Bench testing only; compliance with ANSI S3.22-1987 standard.

## Technological Characteristics

Behind-the-ear form factor; Class D circuitry; telecoil with preamplifier; four fitter controls (power, compression, low/high cut tone); size 13 battery power; ANSI S3.22-1987 compliant.

## Regulatory Identification

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. An air-conduction hearing aid is subject to the requirements in § 800.30 or § 801.422 of this chapter, as applicable. The air-conduction hearing aid generic type excludes the group hearing aid or group auditory trainer, master hearing aid, and the tinnitus masker, regulated under §§ 874.3320, 874.3330, and 874.3400, respectively.

## Submission Summary (Full Text)

> This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com.
>
> Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/).

{0}

UNITRON INDUSTRIES INC. K964508 Nov. 27, 1996

# A Summary of Safety and Effectiveness Information

Name of Device: Unitron Industries, ICON AoHP 4

Type of Device: Behind-The-Ear Hearing Aids. Substantially equivalent to other behind-the-ear hearing aids.

Intended Use: To amplify and transmit sound via air conduction to the ear.

Features:
- Four fitter controls - Power, Compression Limiting, active low cut tone, high cut tone.
- Class D circuitry for excellent battery life.
- Powerful telecoil with preamplifier.

Assembly: Assembled from standard components that are used by Unitron and other hearing aid manufacturers.

Technical Characteristics: Technical specifications comply with ANSI Standard S 3.22-1987.

Controls:
- Volume Control, similar to other devices.
- Switch for selecting microphone, telecoil and off.

Power: Standard hearing aid battery - size 13.

A user's manual and other information is supplied with each hearing aid.

3555 Walnut Street • P.O. Box 5010 • Port Huron, Michigan 48061-5010 • Telephone (810) 982-0166 1-800-521-5400 Fax (810) 987-2011

---

**Source:** [https://fda.innolitics.com/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ESD/K964508](https://fda.innolitics.com/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ESD/K964508)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
