Cordiana Medical Informatics AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Cordiana Medical Informatics AG - FDA 510(k) Cleared Devices
Recent clearances: Cordiana Dx16
1
Total
1
Cleared
0
Denied
Cordiana Medical Informatics AG has 1 FDA 510(k) cleared medical devices. Based in Root, CH.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cordiana Medical Informatics AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cordiana Medical Informatics AG
1 devices