Vascular Logics, Inc.
Country not established
- Devices
- 1
What Vascular Logics, Inc. makes
Vascular Logics, Inc. manufactures the Brannon Arterio-Venous Port-Syringe, a device designed for vascular access procedures.
The company’s portfolio is regulated under FDA Class II devices and includes products listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Brannon Arterio-Venous Portsyringe Ref K965030
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascular Logics, Inc. have in the registry?
The registry currently lists 1 device for Vascular Logics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascular Logics, Inc.'s devices?
Among its 1 most recently registered device, Vascular Logics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vascular Logics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vascular Logics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vascular Logics, Inc. in the registry?
The most recently registered devices listed for Vascular Logics, Inc. include BRANNON ARTERIO-VENOUS PORTSYRINGE.