George Loo, MD
Country not established
- Devices
- 1
What George Loo, MD makes
The manufacturer produces a 4-port, 4-way stopcock, a manual valve used in medical settings to control fluid flow between multiple pathways in infusion or drainage systems.
This device is classified as Class II under FDA regulations and is listed via a 510(k) premarket notification. The company is based in the United States.
Catalogue
4 Port, 4 Way Stopcock Ref K010217
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does George Loo, MD have in the registry?
The registry currently lists 1 device for George Loo, MD. Devices recorded under merged duplicate company entries are counted once.
Which registries list George Loo, MD's devices?
Among its 1 most recently registered device, George Loo, MD has devices listed in FDA 510(k) (1 device).
What risk classes do George Loo, MD's devices fall under?
Among its 1 most recently registered device, the classes recorded for George Loo, MD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from George Loo, MD in the registry?
The most recently registered devices listed for George Loo, MD include 4 PORT, 4 WAY STOPCOCK.