Cardiac Imaging
Country not established
- Devices
- 1
What Cardiac Imaging makes
The company manufactures the Biovision Cardiac Strobe, a device designed for cardiac imaging to enhance visualization of heart structures and function during diagnostic procedures.
This product is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Biovision Cardiac Strobe Ref K811341
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiac Imaging have in the registry?
The registry currently lists 1 device for Cardiac Imaging. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiac Imaging's devices?
Among its 1 most recently registered device, Cardiac Imaging has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiac Imaging's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiac Imaging's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiac Imaging in the registry?
The most recently registered devices listed for Cardiac Imaging include BIOVISION CARDIAC STROBE.