Synopsys (Northern Europe) , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Synopsys (Northern Europe) , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Simpleware ScanIP Medical
1
Total
1
Cleared
0
Denied
Synopsys (Northern Europe) , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Exeter, GB.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Synopsys (Northern Europe) , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Synopsys (Northern Europe) , Ltd.
1 devices