Cardio Metrics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 23
What Cardio Metrics, Inc. makes
Cardio Metrics, Inc. makes cardiovascular monitoring and measurement devices, including continuous cardiac output monitoring systems, perfusion monitors, and Doppler ultrasound instruments such as Flowire Doppler guide wires and FloMAP ultrasound systems. The company also produces intravascular guide wires like the AccuTrac and modified FloCath pulmonary artery catheter, as well as mediastinal autotransfusion systems and related switch boxes and smart wire technologies.
The devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 23 devicesFrequently asked questions
How many devices does Cardio Metrics, Inc. have in the registry?
The registry currently lists 23 devices for Cardio Metrics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio Metrics, Inc.'s devices?
Among its 23 most recently registered devices, Cardio Metrics, Inc. has devices listed in FDA 510(k) (23 devices).
What risk classes do Cardio Metrics, Inc.'s devices fall under?
Among its 23 most recently registered devices, the classes recorded for Cardio Metrics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio Metrics, Inc. in the registry?
The most recently registered devices listed for Cardio Metrics, Inc. include CARDIOMETRICS DUALFLOW SWITCH BOX, CONTINUOUS CARDIAC OUTPUT MONITORING SYSTEM, CARDIOMETRICS SMARTWIRE(TM)/FLOMAP(R) and CARDIOMETRICS FLOWIRE/FLOMAP DOPPLER ULTRASOUND.