Hemodialysis, Division of The
Country not established
- Devices
- 1
What Hemodialysis, Division of The makes
The company manufactures the DLC 500, a double lumen catheter designed for hemodialysis procedures.
This product is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Dlc 500, Double Lumen Catheter Ref K781050
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemodialysis, Division of The have in the registry?
The registry currently lists 1 device for Hemodialysis, Division of The. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemodialysis, Division of The's devices?
Among its 1 most recently registered device, Hemodialysis, Division of The has devices listed in FDA 510(k) (1 device).
What risk classes do Hemodialysis, Division of The's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemodialysis, Division of The's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemodialysis, Division of The in the registry?
The most recently registered devices listed for Hemodialysis, Division of The include DLC 500, DOUBLE LUMEN CATHETER.