Philips 45 Series
FDA 510(k) K933850 · Philips Hearing Instruments Co.
510(k) numberK933850
Submission
- Device name
- Philips 45 Series
- Applicant
- Philips Hearing Instruments Co.
Mahwah, NJ, US - Received
- August 6, 1993
- Decision date
- September 7, 1993
- 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.
Other 510(k)s with product code ESD
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| 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 |
|---|---|---|
| K972818 | D72 DigitalESD · Traditional | 10/17/1997SE |
| K971804 | Philips S1694, S1695ESD · Traditional | 06/06/1997SE |
| K965088 | M11 Series: M11, M11MESD · Traditional | 01/24/1997SE |
| K961770 | Philips 71 SeriesESD · Traditional | 08/02/1996SE |
| K952658 | Hearing AidESD · Traditional | 07/28/1995SE |
| K944404 | MO4 SeriesESD · Traditional | 12/27/1994SE |
| K943670 | MO6 SeriesESD · Traditional | 08/18/1994SE |
| K943395 | Philips M38 SeriesESD · Traditional | 08/09/1994SE |
| K942164 | Philips 61 SeriesESD · Traditional | 06/17/1994SE |
| K921725 | Philip XP Series, In-The Canal Hearing AidESD · Traditional | 08/11/1992SE |
Questions and answers
When was Philips 45 Series cleared by the FDA?
Philips 45 Series (K933850) received a 510(k) decision of Substantially Equivalent on September 7, 1993, 32 days after the submission was received.
What is the product code of K933850?
The FDA product code is ESD – Hearing Aid, Air-Conduction, Prescription, a Class I (low risk) device regulated under 21 CFR 874.3300.