Auditdata A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Auditdata A/S - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Auditdata A/S has 1 FDA 510(k) cleared medical devices. Based in Taastrup, DK.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Auditdata A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Auditdata A/S
1 devices