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.
510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.
1 devices