Clarigen, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dialguard Endotoxin Removal Device Ref K993806
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clarigen, Inc. have in the registry?
The registry currently lists 1 device for Clarigen, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clarigen, Inc.'s devices?
Among its 1 most recently registered device, Clarigen, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Clarigen, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Clarigen, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clarigen, Inc. in the registry?
The most recently registered devices listed for Clarigen, Inc. include DIALGUARD ENDOTOXIN REMOVAL DEVICE.