Diagnostica Stago, Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diagnostica Stago, Incorporated - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Diagnostica Stago, Incorporated has 2 FDA 510(k) cleared medical devices. Based in Parisppany, US.
Historical record: 2 cleared submissions from 2009 to 2013. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Diagnostica Stago, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diagnostica Stago, Incorporated
2 devices