Koo Americas, Inc.
Country not established
- Devices
- 1
Catalogue
Koo Americas Valve Peep, Model Km-809 Ref K050918
510(k) 510(k)
Frequently asked questions
How many devices does Koo Americas, Inc. have in the registry?
The registry currently lists 1 device for Koo Americas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Koo Americas, Inc.'s devices?
Among its 1 most recently registered device, Koo Americas, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Koo Americas, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Koo Americas, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Koo Americas, Inc. in the registry?
The most recently registered devices listed for Koo Americas, Inc. include KOO AMERICAS VALVE PEEP, MODEL KM-809.