Cardiosonix, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Cardiosonix, Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Cardiosonix, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Kfar Saba, IL.
Historical record: 3 cleared submissions from 2002 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiosonix, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiosonix, Ltd.
3 devices