Hemodia Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Hemodia Sas - FDA 510(k) Cleared Devices
Recent clearances: DOUBLEFLO INFLOW/OUTFLOW PUMP, accessories and tubing sets, DOUBLEFLO system, Zeos Aqua Vision Pump and tube
4
Total
4
Cleared
0
Denied
Hemodia Sas has 4 FDA 510(k) cleared medical devices. Based in Labege, FR.
Last cleared in 2023. Active since 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hemodia Sas Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Visamed GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Hemodia Sas
4 devices