Cardiotechnics, Inc.
Country not established
- Devices
- 1
What Cardiotechnics, Inc. makes
Cardiotechnics, Inc. manufactures ambulatory ECG digital monitors, specifically the TD-30 model.
The company is based in the United States, and its devices are classified as Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
Ambulatory Ecg Digital Monitor Model: Td-30 Ref K880615
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiotechnics, Inc. have in the registry?
The registry currently lists 1 device for Cardiotechnics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiotechnics, Inc.'s devices?
Among its 1 most recently registered device, Cardiotechnics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiotechnics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiotechnics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiotechnics, Inc. in the registry?
The most recently registered devices listed for Cardiotechnics, Inc. include AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30.