Augmedit B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Augmedit B.V. - FDA 510(k) Cleared Devices
Recent clearances: LumiNE US
1
Total
1
Cleared
0
Denied
Augmedit B.V. has 1 FDA 510(k) cleared medical devices. Based in Naarden, NL.
Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Augmedit B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Augmedit B.V.
1 devices