Cardio Management, Inc.
Country not established
- Devices
- 1
What Cardio Management, Inc. makes
Cardio Management, Inc. manufactures the CMI 3000, a medical device designed for cardiac monitoring and rhythm analysis, likely used in clinical or outpatient settings to assess heart function and detect arrhythmias.
The company’s portfolio is regulated under FDA Class II devices, with the CMI 3000 authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Cmi 3000 Ref K854233
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardio Management, Inc. have in the registry?
The registry currently lists 1 device for Cardio Management, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio Management, Inc.'s devices?
Among its 1 most recently registered device, Cardio Management, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardio Management, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardio Management, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio Management, Inc. in the registry?
The most recently registered devices listed for Cardio Management, Inc. include CMI 3000.