Medical Device Manufacturer · IL , Kfar Saba

Biosonix , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002
1
Total
1
Cleared
0
Denied

Biosonix , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Kfar Saba, IL.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Biosonix , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biosonix , Ltd.

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