Fysicon BV is one of 137 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Fysicon BV - FDA 510(k) Cleared Devices
Recent clearances: QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid), QMAPP Amplifier
2
Total
2
Cleared
0
Denied
Fysicon BV has 2 FDA 510(k) cleared medical devices. Based in Oss, NL.
Latest FDA clearance: Aug 2025. Active since 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Fysicon BV Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Qserve Group, Us, Inc. and Trisler Consulting.
FDA 510(k) Regulatory Record - Fysicon BV
2 devices