Ars Magna
Country not established
- Devices
- 1
What Ars Magna makes
Ars Magna manufactures the ULTRAPROBE, a medical imaging device designed for diagnostic ultrasound applications, including real-time visualization of internal body structures.
The ULTRAPROBE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Ultraprobe Ref K810133
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ars Magna have in the registry?
The registry currently lists 1 device for Ars Magna. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ars Magna's devices?
Among its 1 most recently registered device, Ars Magna has devices listed in FDA 510(k) (1 device).
What risk classes do Ars Magna's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ars Magna's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ars Magna in the registry?
The most recently registered devices listed for Ars Magna include ULTRAPROBE.