Marcon Group, Inc.
Country not established
- Devices
- 1
What Marcon Group, Inc. makes
Marcon Group, Inc. manufactures the AirCel System, a medical device designed for respiratory support and airway management, including continuous positive airway pressure (CPAP) and bilevel positive airway pressure (BiPAP) therapies.
The AirCel System is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
The Aircel System Ref K954593
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Marcon Group, Inc. have in the registry?
The registry currently lists 1 device for Marcon Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Marcon Group, Inc.'s devices?
Among its 1 most recently registered device, Marcon Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Marcon Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Marcon Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Marcon Group, Inc. in the registry?
The most recently registered devices listed for Marcon Group, Inc. include THE AIRCEL SYSTEM.