Vascular Architects, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Vascular Architects, Inc. makes
Vascular Architects, Inc. makes covered stents and delivery systems for vascular applications, including the Aspire Covered Stent and Controlled Expansion Delivery System, modifications to that system, the Aspire Covered Stent and Delivery Catheter, the Periscope Device, and the Aspire Covered Stent with 718 Delivery System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Modification To Vascular Architects Aspire Covered Stent And Contrilled Expansion Delivery System Ref K030567
Regimes: 510(k) Registry: 510(k)Aspire Covered Stent And Delivery Catheter Ref K003173
Regimes: 510(k) Registry: 510(k)Vascular Architects Periscope Device Ref K003719
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascular Architects, Inc. have in the registry?
The registry currently lists 5 devices for Vascular Architects, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascular Architects, Inc.'s devices?
Among its 5 most recently registered devices, Vascular Architects, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Vascular Architects, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Vascular Architects, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vascular Architects, Inc. in the registry?
The most recently registered devices listed for Vascular Architects, Inc. include VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSION DELIVERY SYSTEM, MODIFICATION TO VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTRILLED EXPANSION DELIVERY SYSTEM, ASPIRE COVERED STENT AND DELIVERY CATHETER and VASCULAR ARCHITECTS PERISCOPE DEVICE.