Cavernosometry Module for Menuet
FDA 510(k) K923117 · Dantec Medical, Inc.
510(k) numberK923117
Submission
- Device name
- Cavernosometry Module for Menuet
- Applicant
- Dantec Medical, Inc.
Washington, DC, US - Received
- June 26, 1992
- Decision date
- February 22, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DXT – Injector And Syringe, Angiographic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1650
- Specialty
- Cardiovascular
Other 510(k)s with product code DXT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252652 | Disposable Syringes with Accessories for Power Injectors (900103T); Disposable Syringes…DXT · Traditional | Fortis Biosolutions Company Limited | 05/14/2026SE |
| K252653 | ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module…DXT · Traditional | Acist Medical Systems, Inc. | 05/13/2026SE |
| K252638 | VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use…DXT · Traditional | Acist Medical Systems, Inc. | 05/13/2026SE |
| K253048 | High Pressure Syringe; Pressure Connecting Tube; Quick fill tube; Spike; Transfer TubeDXT · Traditional | Shenzhen Maiwei Biotech Co., Ltd. | 04/16/2026SE |
| K251788 | Extension tubeDXT · Traditional | Zhuhai DR Medical Instruments Co., Ltd. | 03/05/2026SE |
| K252891 | MEDRAD MRXperion MR Injection System and MR Injection System Syringe Kit; MEDRAD ISI2…DXT · Traditional | Bayer Medical Care, Inc. | 02/13/2026SE |
| K244038 | High Pressure TubingDXT · Traditional | Shandong Int Medical Instruments Co., Ltd. | 09/05/2025SE |
| K242143 | Angiography InjectorDXT · Traditional | Shandong Int Medical Instruments Co., Ltd. | 12/23/2024SE |
| K242212 | Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)DXT · Traditional | Nemoto Kyorindo Co., Ltd. | 08/27/2024SE |
| K241109 | Single-use Sterile High-pressure Angiographic Syringes and AccessoriesDXT · Traditional | Shenzhen Boon Medical Supply Co., Ltd. | 08/22/2024SE |
More from Shenzhen Boon Medical Supply Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
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| K950314 | Dantec Monopolar Lumen Electrode (13R18 and 13R19)GXZ · Traditional | 03/25/1996SE |
| K953999 | Dantec Da CapoEXY · Traditional | 11/21/1995SE |
| K926363 | Multi-Dop SIYO · Traditional | 06/19/1995SE |
| K931801 | Multi-Dop XIYO · Traditional | 06/14/1995SE |
| K930458 | Multi-Dop LIYN · Traditional | 02/03/1995SE |
| K932059 | Needle Electrodes and Disposable Scalp ElectrodeIKT · Traditional | 10/04/1994SE |
| K934580 | Dantec 13R45 Bar ElectrodeGXY · Traditional | 09/26/1994SE |
| K931966 | Dantec Disposable Concentric NeedleIKT · Traditional | 03/30/1994SE |
| K931923 | Dantec Maglite Magnetic Stimulator (Maglite)GWF · Traditional | 11/09/1993SE |
Questions and answers
When was Cavernosometry Module for Menuet cleared by the FDA?
Cavernosometry Module for Menuet (K923117) received a 510(k) decision of Substantially Equivalent on February 22, 1993, 241 days after the submission was received.
What is the product code of K923117?
The FDA product code is DXT – Injector And Syringe, Angiographic, a Class II (moderate risk) device regulated under 21 CFR 870.1650.