Plasmatica, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Plasmatica, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Ra'Anana, IL.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Plasmatica, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
1 devices