Novonx, Inc.
Country not established
- Devices
- 1
What Novonx, Inc. makes
Novonx, Inc. manufactures multi-centrifuge systems designed for processing biological samples, likely in clinical or research settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Multi-Centrifuge Ref K955795
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Novonx, Inc. have in the registry?
The registry currently lists 1 device for Novonx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novonx, Inc.'s devices?
Among its 1 most recently registered device, Novonx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Novonx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Novonx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Novonx, Inc. in the registry?
The most recently registered devices listed for Novonx, Inc. include MULTI-CENTRIFUGE.