Ackermann Instrumente GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Ackermann Instrumente GmbH has 3 FDA 510(k) cleared medical devices. Based in Chesterland, US.
Historical record: 3 cleared submissions from 1998 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ackermann Instrumente GmbH Filter by specialty or product code using the sidebar.
3 devices