Cardiomedix, Inc.
Country not established
- Devices
- 1
What Cardiomedix, Inc. makes
Cardiomedix, Inc. manufactures the ECG SENTINEL System, a device designed for continuous electrocardiogram monitoring to detect and alert on cardiac events in real time.
The ECG SENTINEL System is classified as a Class II medical device and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
ECG SENTINEL System Ref K172801
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiomedix, Inc. have in the registry?
The registry currently lists 1 device for Cardiomedix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiomedix, Inc.'s devices?
Among its 1 most recently registered device, Cardiomedix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiomedix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiomedix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiomedix, Inc. in the registry?
The most recently registered devices listed for Cardiomedix, Inc. include ECG SENTINEL System.