I3 Membrane GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
I3 Membrane GmbH has 1 FDA 510(k) cleared medical devices. Based in Radeberg, DE.
Last cleared in 2023. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by I3 Membrane GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by I3 Membrane GmbH
1 devices