Kholber Corp.
Country not established
- Devices
- 1
What Kholber Corp. makes
Kholber Corp. manufactures the Cardiotrode, a medical device designed for cardiac monitoring or stimulation applications.
The Cardiotrode is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Cardiotrode Ref K840646
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kholber Corp. have in the registry?
The registry currently lists 1 device for Kholber Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kholber Corp.'s devices?
Among its 1 most recently registered device, Kholber Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Kholber Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kholber Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kholber Corp. in the registry?
The most recently registered devices listed for Kholber Corp. include CARDIOTRODE.