Monagan Ent., Inc.
Country not established
- Devices
- 1
What Monagan Ent., Inc. makes
Monagan Ent., Inc. makes the SECOND WIND AIR PURIFIER, a device designed to clean indoor air by removing particulates and contaminants.
The SECOND WIND AIR PURIFIER is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Second Wind Air Purifier Ref K980745
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Monagan Ent., Inc. have in the registry?
The registry currently lists 1 device for Monagan Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Monagan Ent., Inc.'s devices?
Among its 1 most recently registered device, Monagan Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Monagan Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Monagan Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Monagan Ent., Inc. in the registry?
The most recently registered devices listed for Monagan Ent., Inc. include SECOND WIND AIR PURIFIER.