Sonomedica
Country not established
- Devices
- 1
What Sonomedica makes
Sonomedica manufactures the Sonospectrographic Analyzer, a cardiovascular device designed for spectral Doppler analysis of blood flow and cardiac structures. It processes ultrasound signals to generate visual representations of blood flow characteristics, aiding in diagnostic assessments of cardiac function and vascular health.
The company’s portfolio is regulated under FDA Class II devices, with the Sonospectrographic Analyzer authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. Sonomedica is headquartered in the United States.
Catalogue
Cardiovascular Sonospectrographic Analyzer Ref K023759
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonomedica have in the registry?
The registry currently lists 1 device for Sonomedica. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonomedica's devices?
Among its 1 most recently registered device, Sonomedica has devices listed in FDA 510(k) (1 device).
What risk classes do Sonomedica's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sonomedica's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonomedica in the registry?
The most recently registered devices listed for Sonomedica include CARDIOVASCULAR SONOSPECTROGRAPHIC ANALYZER.