Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. is one of 8 FDA 510(k) medical device manufacturers from Slovenia in the dataset, ranked by real submission volume.
Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. - FDA 510(k) ...
Recent clearances: Automated ankle brachial pressure index measuring device, MESI mTABLET system, Automated ankle brachial pressure index measuring device
2
Total
2
Cleared
0
Denied
Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Ljubljana, SI.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd. 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 D.O.O.; Mesi, Development of Medical Devices, Ltd.
2 devices