Diter Elektroniikka Oy
Country not established
- Devices
- 1
What Diter Elektroniikka Oy makes
Diter Elektroniikka OY manufactures the DITER ULTRASONIC S 3000, a Class II ultrasonic device designed for medical imaging or therapeutic applications.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices listed in the United States. The manufacturer is based in the US.
Catalogue
Diter Ultrasonic S 3000 Ref K901950
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diter Elektroniikka OY have in the registry?
The registry currently lists 1 device for Diter Elektroniikka OY. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diter Elektroniikka OY's devices?
Among its 1 most recently registered device, Diter Elektroniikka OY has devices listed in FDA 510(k) (1 device).
What risk classes do Diter Elektroniikka OY's devices fall under?
Among its 1 most recently registered device, the classes recorded for Diter Elektroniikka OY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diter Elektroniikka OY in the registry?
The most recently registered devices listed for Diter Elektroniikka OY include DITER ULTRASONIC S 3000.