Perfaction, Inc.
Country not established
- Devices
- 1
What Perfaction, Inc. makes
Perfaction, Inc. manufactures the AIRGENT system (Model AG7000010), a medical device designed for respiratory therapy, including the delivery of aerosolized medications and humidification for patients.
The company’s portfolio is regulated under FDA Class II devices, with the AIRGENT system authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Airgent, Model AG7000010 Ref K082138
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perfaction, Inc. have in the registry?
The registry currently lists 1 device for Perfaction, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perfaction, Inc.'s devices?
Among its 1 most recently registered device, Perfaction, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Perfaction, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Perfaction, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perfaction, Inc. in the registry?
The most recently registered devices listed for Perfaction, Inc. include AIRGENT, MODEL AG7000010.