Clinisurg Vascular Products, LLC
Country not established
- Devices
- 1
What Clinisurg Vascular Products, LLC makes
Clinisurg Vascular Products, LLC manufactures the C-PORT, a vascular access port designed for repeated intravenous or subcutaneous drug administration and fluid infusion.
The C-PORT is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
C-Port Ref K030636
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinisurg Vascular Products, LLC have in the registry?
The registry currently lists 1 device for Clinisurg Vascular Products, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinisurg Vascular Products, LLC's devices?
Among its 1 most recently registered device, Clinisurg Vascular Products, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Clinisurg Vascular Products, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Clinisurg Vascular Products, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinisurg Vascular Products, LLC in the registry?
The most recently registered devices listed for Clinisurg Vascular Products, LLC include C-PORT.