Rocky Mountain Biosystems, Inc.
Country not established
- Devices
- 1
What Rocky Mountain Biosystems, Inc. makes
Rocky Mountain Biosystems, Inc. manufactures the BioFusionary BEBE, a Class II medical device designed for blood component processing and separation.
The BioFusionary BEBE is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Biofusionary Bebe Ref K121123
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rocky Mountain Biosystems, Inc. have in the registry?
The registry currently lists 1 device for Rocky Mountain Biosystems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rocky Mountain Biosystems, Inc.'s devices?
Among its 1 most recently registered device, Rocky Mountain Biosystems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rocky Mountain Biosystems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rocky Mountain Biosystems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rocky Mountain Biosystems, Inc. in the registry?
The most recently registered devices listed for Rocky Mountain Biosystems, Inc. include BIOFUSIONARY BEBE.