Vascular Intervention
Country not established
- Devices
- 1
What Vascular Intervention makes
The company manufactures peripheral dilatation catheters, including over-the-wire (OTW) designs, and biliary self-expanding metal stents (SEMS). These devices are intended for vascular and biliary interventions, such as dilating narrowed blood vessels and supporting bile ducts.
The portfolio consists of Class II medical devices, authorised via the FDA’s 510(k) pathway. These products are listed in the FDA’s 510(k) database and comply with US regulatory requirements. The company operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascular Intervention have in the registry?
The registry currently lists 1 device for Vascular Intervention. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascular Intervention's devices?
Among its 1 most recently registered device, Vascular Intervention has devices listed in FDA 510(k) (1 device).
What risk classes do Vascular Intervention's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vascular Intervention's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vascular Intervention in the registry?
The most recently registered devices listed for Vascular Intervention include RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, OTW VIATRAC 18 PERIPHERAL DILATATION CATHETER, RX HERCULINK 14 BILIARY STN.