Diagnostica-Stago is one of 13268 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diagnostica-Stago - FDA 510(k) Cleared Devices
Recent clearances: STA® - Liatest® D-Di, STA LIATEST D-DI
3
Total
3
Cleared
0
Denied
Diagnostica-Stago has 3 FDA 510(k) cleared medical devices. Based in Parisppany, US.
Historical record: 3 cleared submissions from 2001 to 2016. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Diagnostica-Stago Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Diagnostica Stago and Donawa Lifescience Consulting. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Diagnostica-Stago
3 devices