Diacardio, Ltd.
Country not established
- Devices
- 2
What Diacardio, Ltd. makes
Diacardio, Ltd. manufactures the LVivo Software Application, a digital tool for electrophysiological analysis, and the LVIVO EF SYSTEM, a hardware-software combination for cardiac electrophysiology studies and ablation procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The manufacturer is based in the United States.
Catalogue
LVivo Software Application Ref K161382
Regimes: 510(k) Registry: 510(k)Lvivo Ef System Ref K130779
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diacardio, Ltd. have in the registry?
The registry currently lists 2 devices for Diacardio, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diacardio, Ltd.'s devices?
Among its 2 most recently registered devices, Diacardio, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Diacardio, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Diacardio, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diacardio, Ltd. in the registry?
The most recently registered devices listed for Diacardio, Ltd. include LVivo Software Application and LVIVO EF SYSTEM.