Cardiox Corp.
Country not established
- Devices
- 1
What Cardiox Corp. makes
Cardiox Corp. manufactures the Cardiox Flow Detection System, a device designed for monitoring and detecting blood flow in cardiovascular applications, likely used in clinical or procedural settings to assess perfusion dynamics.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Cardiox Flow Detection System Ref K122400
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiox Corp. have in the registry?
The registry currently lists 1 device for Cardiox Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiox Corp.'s devices?
Among its 1 most recently registered device, Cardiox Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiox Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiox Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiox Corp. in the registry?
The most recently registered devices listed for Cardiox Corp. include CARDIOX FLOW DETECTION SYSTEM.