Diasorin is one of 13100 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diasorin - FDA 510(k) Cleared Devices
Recent clearances: LIAISON ALDOSTERONE, LIAISON ALDOSTERONE CONTROL SET, LIAISON ALDOSTERONE CALIBRATION VERIFIERS
1
Total
1
Cleared
0
Denied
Diasorin has 1 FDA 510(k) cleared medical devices. Based in Stillwater, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Diasorin Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diasorin
1 devices