Delphi Consulting Group
Country not established
- Devices
- 6
What Delphi Consulting Group makes
Delphi Consulting Group manufactures venous thromboembolism (VTE) prevention devices, including pneumatic compression systems like the TRINITY DVT System and TRINITY II Single Chamber DVT Pump, as well as compatible sleeves for use with Huntleigh pumps. Their portfolio also includes electronic auscultation tools, such as the E-SCOPE Electronic Stethoscope and SIMULSCOPE auscultation systems for bedside use.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. Their products are based in the United States.
Catalogue
Trinity Dvt System Ref K963957
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Trinity Ii Single Chamber Dvt Pump Ref K983680
Regimes: 510(k) Registry: 510(k)E-Scope Electronic Stethoscope Model 718-7120 Ref K961301
Regimes: 510(k) Registry: 510(k)Trinity Sleeve(S) Ref K954489
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Delphi Consulting Group have in the registry?
The registry currently lists 6 devices for Delphi Consulting Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Delphi Consulting Group's devices?
Among its 6 most recently registered devices, Delphi Consulting Group has devices listed in FDA 510(k) (6 devices).
What risk classes do Delphi Consulting Group's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Delphi Consulting Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Delphi Consulting Group in the registry?
The most recently registered devices listed for Delphi Consulting Group include TRINITY DVT SYSTEM, TRINITY SLEEVES, HUNTLEIGH PUMP COMPATIBLE(T.B.D.), TRINITY II SINGLE CHAMBER DVT PUMP and E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120.