Mesi D.O.O. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mesi D.O.O. has 1 FDA 510(k) cleared medical devices. Based in Ljubljana, SI.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Mesi D.O.O. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mesi D.O.O.
1 devices