Leaseir Technologies, Slu - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Leaseir Technologies, Slu has 1 FDA 510(k) cleared medical devices. Based in Gij?n, ES.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Leaseir Technologies, Slu Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Freyr Global Regulatory Solutions and Services as regulatory consultant.
1 devices