Dimeco
Country not established
- Devices
- 1
What Dimeco makes
Dimeco makes the CLINIC 2000 MODEL MULTI-FRECODYN DEVICE, which is a multi-frequency electrotherapy device used for clinical applications.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Clinic 2000 Model Multi-Frecodyn Device Ref K820784
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dimeco have in the registry?
The registry currently lists 1 device for Dimeco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dimeco's devices?
Among its 1 most recently registered device, Dimeco has devices listed in FDA 510(k) (1 device).
What risk classes do Dimeco's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dimeco's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dimeco in the registry?
The most recently registered devices listed for Dimeco include CLINIC 2000 MODEL MULTI-FRECODYN DEVICE.