Kai Medtech, LLC
Country not established
- Devices
- 1
What Kai Medtech, LLC makes
Kai Medtech, LLC manufactures the Minjie Catheter System, a medical device designed for specific vascular or interventional procedures.
The Minjie Catheter System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Minjie Catheter System Ref K212288
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kai Medtech, LLC have in the registry?
The registry currently lists 1 device for Kai Medtech, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kai Medtech, LLC's devices?
Among its 1 most recently registered device, Kai Medtech, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Kai Medtech, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kai Medtech, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kai Medtech, LLC in the registry?
The most recently registered devices listed for Kai Medtech, LLC include Minjie Catheter System.