Diacoustic Medical (Pty)
Country not established
- Devices
- 1
What Diacoustic Medical (Pty) makes
Diacoustic Medical produces the SENSICARDIAC, a device designed for cardiac monitoring and diagnostic purposes, likely incorporating acoustic or sensor-based technology to assess heart function or detect abnormalities.
The SENSICARDIAC is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Sensicardiac Ref K121617
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diacoustic Medical (Pty) have in the registry?
The registry currently lists 1 device for Diacoustic Medical (Pty). Devices recorded under merged duplicate company entries are counted once.
Which registries list Diacoustic Medical (Pty)'s devices?
Among its 1 most recently registered device, Diacoustic Medical (Pty) has devices listed in FDA 510(k) (1 device).
What risk classes do Diacoustic Medical (Pty)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Diacoustic Medical (Pty)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diacoustic Medical (Pty) in the registry?
The most recently registered devices listed for Diacoustic Medical (Pty) include SENSICARDIAC.