Kontron Elektronik GmbH
Country not established
- Devices
- 1
What Kontron Elektronik GmbH makes
Kontron Elektronik GmbH manufactures the CARDIO 500, a medical device designed for cardiac monitoring and diagnostic purposes, likely including real-time electrocardiogram (ECG) recording and analysis.
The CARDIO 500 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
Cardio 500 Ref K913754
510(k) 510(k)
Frequently asked questions
How many devices does Kontron Elektronik GmbH have in the registry?
The registry currently lists 1 device for Kontron Elektronik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kontron Elektronik GmbH's devices?
Among its 1 most recently registered device, Kontron Elektronik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Kontron Elektronik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kontron Elektronik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kontron Elektronik GmbH in the registry?
The most recently registered devices listed for Kontron Elektronik GmbH include CARDIO 500.