Sanolla , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sanolla , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Nesher, IL.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sanolla , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Sanolla , Ltd.
1 devices