Eckert & Ziegler Bebig GmbH - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Eckert & Ziegler Bebig GmbH has 4 FDA 510(k) cleared medical devices. Based in Veenendaal, NL.
Historical record: 4 cleared submissions from 2013 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Eckert & Ziegler Bebig GmbH Filter by specialty or product code using the sidebar.
4 devices