Eg&G Berthold is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Eg&G Berthold - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Eg&G Berthold has 1 FDA 510(k) cleared medical devices. Based in Germany, DE.
Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Eg&G Berthold Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eg&G Berthold
1 devices