Dualams, Inc., Dba Airkor
Country not established
- Devices
- 1
What Dualams, Inc., Dba Airkor makes
Dualams, Inc., Dba Airkor makes the UltraEzAir® (UEA1A) device.
The UltraEzAir® (UEA1A) is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
UltraEzAir® (UEA1A) Ref K240114
510(k) 510(k)
Frequently asked questions
How many devices does Dualams, Inc., Dba Airkor have in the registry?
The registry currently lists 1 device for Dualams, Inc., Dba Airkor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dualams, Inc., Dba Airkor's devices?
Among its 1 most recently registered device, Dualams, Inc., Dba Airkor has devices listed in FDA 510(k) (1 device).
What risk classes do Dualams, Inc., Dba Airkor's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dualams, Inc., Dba Airkor's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dualams, Inc., Dba Airkor in the registry?
The most recently registered devices listed for Dualams, Inc., Dba Airkor include UltraEzAir® (UEA1A).