Hypertension Diagnostics, Inc.
Country not established
- Devices
- 1
What Hypertension Diagnostics, Inc. makes
Hypertension Diagnostics, Inc. manufactures the CVPROFILOR D0-2020 Cardiovascular Profiling System, a device designed for assessing cardiovascular health metrics.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hypertension Diagnostics, Inc. have in the registry?
The registry currently lists 1 device for Hypertension Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hypertension Diagnostics, Inc.'s devices?
Among its 1 most recently registered device, Hypertension Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hypertension Diagnostics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hypertension Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hypertension Diagnostics, Inc. in the registry?
The most recently registered devices listed for Hypertension Diagnostics, Inc. include CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM.