Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. is one of 8 FDA 510(k) medical device manufacturers from Slovenia in the dataset, ranked by real submission volume.
Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. - FDA 510(k) ...
Recent clearances: MESI mTablet ECG Diagnostic System, MESI mTablet ECG, MESI mTABLET TBI diagnostic system, MESI mTABLET TBI
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.
510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.
2 devices