Fusmobile, Inc
Country not established FDA establishment FEI 3019585303
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Neurolyser XR (NXR100) Ref DEN250015
De Novo 510(k)
Company details
- FDA FEI number
- 3019585303
- Address
- 6120 Windward Pkwy Ste 210, Alpharetta, GA, 30005
Frequently asked questions
How many devices does FUSMOBILE, INC have in the registry?
The registry currently lists 1 device for FUSMOBILE, INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list FUSMOBILE, INC's devices?
Among its 1 most recently registered device, FUSMOBILE, INC has devices listed in FDA 510(k) (1 device).
What risk classes do FUSMOBILE, INC's devices fall under?
Among its 1 most recently registered device, the classes recorded for FUSMOBILE, INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from FUSMOBILE, INC in the registry?
The most recently registered devices listed for FUSMOBILE, INC include Neurolyser XR (NXR100).