Besam, Inc.
Country not established
- Devices
- 1
What Besam, Inc. makes
Besam, Inc. manufactures the COMBI, a medical device designed for [specific clinical purpose or function—if unspecified, omit or clarify as 'a Class II device intended for [general use, e.g., diagnostic, therapeutic, or monitoring applications]'].
The COMBI is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Combi Ref K840624
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Besam, Inc. have in the registry?
The registry currently lists 1 device for Besam, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Besam, Inc.'s devices?
Among its 1 most recently registered device, Besam, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Besam, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Besam, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Besam, Inc. in the registry?
The most recently registered devices listed for Besam, Inc. include COMBI.