Qompium NV is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Qompium NV - FDA 510(k) Cleared Devices
Recent clearances: FibriCheck, FibriCheck
2
Total
2
Cleared
0
Denied
Qompium NV has 2 FDA 510(k) cleared medical devices. Based in Hasselt, BE.
Latest FDA clearance: Jun 2024. Active since 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Qompium NV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Qompium NV
2 devices