Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB - FDA 510(k) Clear...
1
Total
1
Cleared
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Denied
Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB has 1 FDA 510(k) cleared medical devices. Based in Berlin, DE.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB
1 devices