Eckert & Ziegler Bebig GmbH is one of 144 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Eckert & Ziegler Bebig GmbH - FDA 510(k) Cleared Devices
Recent clearances: SAGIPLAN, SAGIPLAN PROSTATE MODULE ADD ON, SAGIPLAN INCLUDING PROSTATE MODULE, SagiNova, ISOSEED
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.
510(k) submissions have been managed by Capamed, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Eckert & Ziegler Bebig GmbH
4 devices