Kager Intl.
Country not established
- Devices
- 1
What Kager Intl. makes
Kager Intl. manufactures the Kager TrapDust, a device designed for capturing and containing airborne particles, such as dust, in medical or laboratory environments to prevent contamination.
The company’s products are regulated under FDA 510(k) clearance and are listed in the U.S. regulatory database. Kager Intl. is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Kager Trapdust Ref K790085
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kager Intl. have in the registry?
The registry currently lists 1 device for Kager Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kager Intl.'s devices?
Among its 1 most recently registered device, Kager Intl. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Kager Intl. in the registry?
The most recently registered devices listed for Kager Intl. include KAGER TRAPDUST.