Am 260 K-Amp
FDA 510(k) K953052 · Electone, Inc.
510(k) numberK953052
Submission
- Device name
- Am 260 K-Amp
- Applicant
- Electone, Inc.
Longwood, FL, US - Received
- June 30, 1995
- Decision date
- August 15, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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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|---|---|---|---|
| K232999 | Lyric4 Hearing AidESD · Traditional | Sonova AG | 04/11/2024SE |
| K130790 | LYRIC2ESD · Traditional | Phonak, LLC | 06/27/2013SE |
| K081136 | Lyric Hearing AidESD · Traditional | Insound Medical, Inc. | 05/08/2008SE |
| K021867 | Insound XT Series Hearing AidESD · Traditional | Insound Medical, Inc. | 11/19/2002SE |
| K003558 | Tci Combi (Tinnitus Control Instrument Combination)ESD · Traditional | Siemens Hearing Instruments, Inc. | 04/24/2001SE |
| K984518 | Sonic Innovations Completely-In-The-Canal DSP Hearing Aid with Soft ShellESD · Traditional | Sonic Innovations, Inc. | 03/12/1999SE |
| K974751 | Tranquil Tri-Oe, Tranquil Tri-Coe, Tranquil Tri-CicESD · Traditional | General Hearing Instruments, Inc. | 03/06/1998SE |
| K974242 | Argosy Programmable OnqueESD · Traditional | Argosy Electronics | 01/20/1998SE |
| K973880 | Sonix Hearing Aid Fitting and Programming SystemESD · Traditional | Sonix Technologies, Inc. | 01/12/1998SE |
| K974211 | Opus 2 - Full Concha Series - IteESD · Traditional | Bernafon-Maico, Inc. | 12/15/1997SE |
More from Bernafon-Maico, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K973266 | Z Deq-IiESD · Traditional | 09/23/1997SE |
| K961084 | Am 400ESD · Traditional | 04/18/1996SE |
| K955702 | Sonata U-01ESD · Traditional | 02/22/1996SE |
| K953050 | Z33ESD · Traditional | 08/22/1995SE |
| K953047 | Z20ESD · Traditional | 08/22/1995SE |
| K953054 | Am 260 OhmESD · Traditional | 08/15/1995SE |
| K953053 | Am 260 PPESD · Traditional | 08/15/1995SE |
| K953051 | Z35ESD · Traditional | 08/15/1995SE |
| K953049 | Z24ESD · Traditional | 08/15/1995SE |
| K953048 | Z22ESD · Traditional | 08/15/1995SE |
Questions and answers
When was Am 260 K-Amp cleared by the FDA?
Am 260 K-Amp (K953052) received a 510(k) decision of Substantially Equivalent on August 15, 1995, 46 days after the submission was received.
What is the product code of K953052?
The FDA product code is ESD – Hearing Aid, Air-Conduction, Prescription, a Class I (low risk) device regulated under 21 CFR 874.3300.