Acta Vascular Systems, Inc.
Country not established
- Devices
- 1
What Acta Vascular Systems, Inc. makes
Acta Vascular Systems, Inc. manufactures PVA embolization particles, specifically the Ultra Ivalon and Ultra Drivalon product lines. These devices are used for embolization procedures.
The company is based in the United States and maintains a portfolio of Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acta Vascular Systems, Inc. have in the registry?
The registry currently lists 1 device for Acta Vascular Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acta Vascular Systems, Inc.'s devices?
Among its 1 most recently registered device, Acta Vascular Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Acta Vascular Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Acta Vascular Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acta Vascular Systems, Inc. in the registry?
The most recently registered devices listed for Acta Vascular Systems, Inc. include ULTRA IVALON AND ULTRA DRIVALON PVA EMBOLIZATION PARTICLES.