Diacardio, Ltd. is one of 19099 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diacardio, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LVivo Software Application, LVIVO EF SYSTEM
2
Total
2
Cleared
0
Denied
Diacardio, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Somerset, US.
Historical record: 2 cleared submissions from 2013 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Diacardio, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medicsense USA as regulatory consultant.
FDA 510(k) Regulatory Record - Diacardio, Ltd.
2 devices