Phoenix Technology Group, Inc. Dba Phoenix Clinical
Country not established
- Devices
- 1
What Phoenix Technology Group, Inc. Dba Phoenix Clinical makes
Phoenix Clinical manufactures the Phoenix Clinical ICON, a device designed for clinical monitoring and data acquisition in medical research settings, supporting real-time patient parameter tracking and study documentation.
The Phoenix Clinical ICON is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Phoenix Clinical ICON Ref K170527
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phoenix Technology Group, Inc. Dba Phoenix Clinical have in the registry?
The registry currently lists 1 device for Phoenix Technology Group, Inc. Dba Phoenix Clinical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phoenix Technology Group, Inc. Dba Phoenix Clinical's devices?
Among its 1 most recently registered device, Phoenix Technology Group, Inc. Dba Phoenix Clinical has devices listed in FDA 510(k) (1 device).
What risk classes do Phoenix Technology Group, Inc. Dba Phoenix Clinical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Phoenix Technology Group, Inc. Dba Phoenix Clinical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Phoenix Technology Group, Inc. Dba Phoenix Clinical in the registry?
The most recently registered devices listed for Phoenix Technology Group, Inc. Dba Phoenix Clinical include Phoenix Clinical ICON.