Diagnostica Stago S.A.S - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Diagnostica Stago S.A.S has 3 FDA 510(k) cleared medical devices. Based in Gennevilliers, FR.
Last cleared in 2023. Active since 2015. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Diagnostica Stago S.A.S Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Diagnostica Stago, Inc. as regulatory consultant.
3 devices