A0kfusion Systems, Inc.
Country not established
- Devices
- 1
What A0kfusion Systems, Inc. makes
A0kfusion Systems, Inc. manufactures the Model 1001 medical device.
The company is based in the United States, and its product is classified as a Class II medical device listed under the FDA 510(k) regulatory pathway.
Catalogue
Model 1001 Ref K844718
510(k) 510(k)
Frequently asked questions
How many devices does A0kfusion Systems, Inc. have in the registry?
The registry currently lists 1 device for A0kfusion Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list A0kfusion Systems, Inc.'s devices?
Among its 1 most recently registered device, A0kfusion Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do A0kfusion Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for A0kfusion Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A0kfusion Systems, Inc. in the registry?
The most recently registered devices listed for A0kfusion Systems, Inc. include MODEL 1001.