Diagnostica Stago S.A.S is one of 271 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Diagnostica Stago S.A.S - FDA 510(k) Cleared Devices
Recent clearances: STA R Max 3, STA Compact Max 3, STA- NeoPTimal, STA R MAX
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.
Regulatory submissions have been managed by Diagnostica Stago, Inc. and Diagnostica Stago, Incorporated.
FDA 510(k) Regulatory Record - Diagnostica Stago S.A.S
3 devices