Ampronix, Inc.
Country not established
- Devices
- 1
What Ampronix, Inc. makes
Ampronix, Inc. manufactures the MODALIXX, a medical imaging device designed for diagnostic ultrasound applications, including real-time visualization and imaging of internal body structures.
The MODALIXX is classified as a Class II device under FDA regulations and has been authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
Modalixx Ref K110108
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ampronix, Inc. have in the registry?
The registry currently lists 1 device for Ampronix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ampronix, Inc.'s devices?
Among its 1 most recently registered device, Ampronix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ampronix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ampronix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ampronix, Inc. in the registry?
The most recently registered devices listed for Ampronix, Inc. include MODALIXX.