Phoenix Imaging
Country not established
- Devices
- 2
What Phoenix Imaging makes
Phoenix Imaging manufactures diagnostic ultrasound equipment, including the AI 5200 Diagnostic Ultrasound System and its associated AI 5200 Ultrasound Transducer.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Ai 5200 Diagnostic Ultrasound System Ref K880839
Regimes: 510(k) Registry: 510(k)Resubmitted Ai 5200 Ultrasound Transducer Ref K883845
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phoenix Imaging have in the registry?
The registry currently lists 2 devices for Phoenix Imaging. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phoenix Imaging's devices?
Among its 2 most recently registered devices, Phoenix Imaging has devices listed in FDA 510(k) (2 devices).
What risk classes do Phoenix Imaging's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Phoenix Imaging's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Phoenix Imaging in the registry?
The most recently registered devices listed for Phoenix Imaging include AI 5200 DIAGNOSTIC ULTRASOUND SYSTEM and RESUBMITTED AI 5200 ULTRASOUND TRANSDUCER.