Ultrasonix, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ultrasonix, Inc. makes
Ultrasonix, Inc. makes modified ultrasound scanners, including the Modified Radius model MM 5000 and the 750 SD Ultrasound Scanner (Modification).
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
Modified Radius - Model Number Mm 5000 Ref K871727
Regimes: 510(k) Registry: 510(k)750 Sd Ultrasound Scanner(Modification) Ref K851901
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultrasonix, Inc. have in the registry?
The registry currently lists 2 devices for Ultrasonix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultrasonix, Inc.'s devices?
Among its 2 most recently registered devices, Ultrasonix, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ultrasonix, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ultrasonix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultrasonix, Inc. in the registry?
The most recently registered devices listed for Ultrasonix, Inc. include MODIFIED RADIUS - MODEL NUMBER MM 5000 and 750 SD ULTRASOUND SCANNER(MODIFICATION).