Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. - FDA 510(k) ...
2
Total
2
Cleared
0
Denied
Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. has 2 FDA 510(k) cleared medical devices. Based in Ljubljana, SI.
Last cleared in 2023. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mesi, Development of Medical Devices,...
2 devices