Dekumed, Kunststofftechnik Degler GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Dekumed, Kunststofftechnik Degler GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dekumed, Kunststofftechnik Degler GmbH has 1 FDA 510(k) cleared medical devices. Based in Germany, DE.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dekumed, Kunststofftechnik Degler GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dekumed, Kunststofftechnik Degler GmbH
1 devices