Ulrich Alber GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Ulrich Alber GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ulrich Alber GmbH has 1 FDA 510(k) cleared medical devices. Based in Albstadt-Tailfingen, DE.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Ulrich Alber GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ulrich Alber GmbH
1 devices