D. Eugene Hokanson
Country not established
- Devices
- 1
What D. Eugene Hokanson makes
D. Eugene Hokanson manufactures the P-1 Ultrasonic Arteriograph, a diagnostic device used for non-invasive assessment of blood flow in arteries through Doppler ultrasound technology.
The P-1 Ultrasonic Arteriograph is classified as a Class II medical device in the US and is listed under FDA’s 510(k) clearance process. The manufacturer operates from the United States.
Catalogue
P-1 Ultrasonic Arteriograph Ref K761288
510(k) 510(k)
Frequently asked questions
How many devices does D. Eugene Hokanson have in the registry?
The registry currently lists 1 device for D. Eugene Hokanson. Devices recorded under merged duplicate company entries are counted once.
Which registries list D. Eugene Hokanson's devices?
Among its 1 most recently registered device, D. Eugene Hokanson has devices listed in FDA 510(k) (1 device).
What risk classes do D. Eugene Hokanson's devices fall under?
Among its 1 most recently registered device, the classes recorded for D. Eugene Hokanson's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D. Eugene Hokanson in the registry?
The most recently registered devices listed for D. Eugene Hokanson include P-1 ULTRASONIC ARTERIOGRAPH.