Applied Vascular
Country not established
- Devices
- 2
What Applied Vascular makes
Applied Vascular manufactures intravascular catheters, including the AVD INTIMAX™ biliary catheter for biliary drainage and diagnostic intravascular catheters for vascular access and imaging.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Avd Intimax (Tm) Biliary Catheter Ref K910006
Regimes: 510(k) Registry: 510(k)Diagnostic Intravascular Catheter Ref K923699
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Applied Vascular have in the registry?
The registry currently lists 2 devices for Applied Vascular. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Vascular's devices?
Among its 2 most recently registered devices, Applied Vascular has devices listed in FDA 510(k) (2 devices).
What risk classes do Applied Vascular's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Applied Vascular's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Vascular in the registry?
The most recently registered devices listed for Applied Vascular include AVD INTIMAX (TM) BILIARY CATHETER and DIAGNOSTIC INTRAVASCULAR CATHETER.