Aeromax Technologies, Inc.
Country not established
- Devices
- 1
What Aeromax Technologies, Inc. makes
Aeromax Technologies, Inc. manufactures the RITEFLO SPACER, a device designed to assist with the administration of inhaled medications, improving delivery accuracy for respiratory treatments.
The RITEFLO SPACER is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Riteflo Spacer Ref K984085
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aeromax Technologies, Inc. have in the registry?
The registry currently lists 1 device for Aeromax Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aeromax Technologies, Inc.'s devices?
Among its 1 most recently registered device, Aeromax Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aeromax Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aeromax Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aeromax Technologies, Inc. in the registry?
The most recently registered devices listed for Aeromax Technologies, Inc. include RITEFLO SPACER.