Applied Vascular Engineering, Inc.
Country not established
- Devices
- 1
What Applied Vascular Engineering, Inc. makes
Applied Vascular Engineering, Inc. manufactures the AVE ALLIANCE DILATATION CATHETER, a device used for vascular dilation procedures to treat narrowed or blocked arteries.
The company’s portfolio is regulated under Class II devices in the US, with the AVE ALLIANCE DILATATION CATHETER authorised via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Ave Alliance Dilatation Catheter Ref K931384
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Applied Vascular Engineering, Inc. have in the registry?
The registry currently lists 1 device for Applied Vascular Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Vascular Engineering, Inc.'s devices?
Among its 1 most recently registered device, Applied Vascular Engineering, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Applied Vascular Engineering, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Applied Vascular Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Vascular Engineering, Inc. in the registry?
The most recently registered devices listed for Applied Vascular Engineering, Inc. include AVE ALLIANCE DILATATION CATHETER.