Visiomed AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visiomed AG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Visiomed AG has 1 FDA 510(k) cleared medical devices. Based in South West Ranches, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Visiomed AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Visiomed AG
1 devices