Ulrich Alber GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Ulrich Alber GmbH - FDA 510(k) Cleared Devices
Recent clearances: ADVENTURE A10
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.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ulrich Alber GmbH
1 devices