Accent
FDA 510(k) K050693 · Air Techniques, Inc.
510(k) numberK050693
Submission
- Device name
- Accent
- Applicant
- Air Techniques, Inc.
Hicksville, NY, US - Received
- March 17, 2005
- Decision date
- May 26, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Other 510(k)s with product code MUH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K251793 | SOTA Cloud Smart Sensor (1.5)MUH · Traditional | Sota Cloud Corp. | 03/03/2026SE |
| K252570 | EzSensor HD, EzSensor UHDMUH · Special | Qpix Solutions, Inc. | 11/10/2025SE |
| K250687 | Cocoon Solo (DX-7020s)MUH · Traditional | Dexcowin Global, Inc. | 10/24/2025SE |
| K251206 | Digital X-Ray DentiMax Pro Imaging SystemMUH · Traditional | Dentimax, Inc. | 09/24/2025SE |
| K240040 | VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan…MUH · Traditional | VATECH Co., Ltd. | 10/25/2024SE |
| K242778 | X Sensor (Model: IOS-A15IF, HDI-15DGF)MUH · Special | Qpix Solutions, Inc. | 10/11/2024SE |
| K241649 | DUO1 and DUO2MUH · Traditional | Zinnovi, Inc. | 07/05/2024SE |
| K232325 | RAYSCAN a-ExpertMUH · Traditional | Ray Co., Ltd. | 04/18/2024SE |
| K231660 | Digital image scanner of dentalMUH · Traditional | Jiangsu Dynamic Medical Technology Co., Ltd. | 12/20/2023SE |
| K233053 | DEXIS Ti2 Intraoral Sensor, DEXIS IXS Size 1 Intraoral Sensor, DEXIS IXS Size 2…MUH · Traditional | Dental Imaging Technologies Corporation | 11/21/2023SE |
More from Dental Imaging Technologies Corporation
| 510(k) | Device | Decision |
|---|---|---|
| K191623 | ScanX Touch/ScanX Duo TouchMUH · Traditional | 08/21/2019SE |
| K190949 | ScanX Barrier EnvelopesPEM · Traditional | 07/26/2019SE |
| K101289 | Scanx D5000 Series Scanner Model: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QBMQB · Traditional | 08/03/2010SE |
| K090169 | Spectra Fluorescence Caries Detection DeviceNBL · Traditional | 08/18/2009SE |
| K052271 | RinsendoNYL · Traditional | 05/26/2006SE |
| K042397 | Scanx 14MQB · Special | 10/05/2004SE |
| K042266 | AcclaimNRD · Special | 08/31/2004SE |
| K031198 | Scanx 10MQB · Traditional | 06/20/2003SE |
| K024285 | A/T X-Ray 70EHD · Traditional | 04/16/2003SE |
| K013893 | ScanxMUH · Traditional | 02/01/2002SE |
Questions and answers
When was Accent cleared by the FDA?
Accent (K050693) received a 510(k) decision of Substantially Equivalent on May 26, 2005, 70 days after the submission was received.
What is the product code of K050693?
The FDA product code is MUH – System, X-Ray, Extraoral Source, Digital, a Class II (moderate risk) device regulated under 21 CFR 872.1800.