Maui Imaging
Country not established
- Devices
- 1
What Maui Imaging makes
Maui Imaging manufactures the K3900 Ultrasound Imaging System, a diagnostic device used for real-time ultrasound imaging to visualize internal body structures such as organs, tissues, and blood flow.
The K3900 Ultrasound Imaging System is classified as a Class II medical device and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
K3900 Ultrasound Imaging System Ref K230511
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maui Imaging have in the registry?
The registry currently lists 1 device for Maui Imaging. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maui Imaging's devices?
Among its 1 most recently registered device, Maui Imaging has devices listed in FDA 510(k) (1 device).
What risk classes do Maui Imaging's devices fall under?
Among its 1 most recently registered device, the classes recorded for Maui Imaging's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maui Imaging in the registry?
The most recently registered devices listed for Maui Imaging include K3900 Ultrasound Imaging System.