Ultratek
Country not established
- Devices
- 1
What Ultratek makes
Ultratek manufactures ULTRACAST, a medical device designed for ultrasound-guided procedures, likely including imaging or therapeutic applications in interventional radiology or diagnostic settings.
The ULTRACAST device falls under FDA Class II regulation and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ultracast Ref K862499
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultratek have in the registry?
The registry currently lists 1 device for Ultratek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultratek's devices?
Among its 1 most recently registered device, Ultratek has devices listed in FDA 510(k) (1 device).
What risk classes do Ultratek's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ultratek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultratek in the registry?
The most recently registered devices listed for Ultratek include ULTRACAST.