Mgb Endoskopische Gerate GmbH (Berlin) is one of 440 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Mgb Endoskopische Gerate GmbH (Berlin) - FDA 510(k) Cleared Devices
Recent clearances: LAPORT, MGB DISPOSABLE RETRIEVAL BAG LAPBAG
4
Total
4
Cleared
0
Denied
Mgb Endoskopische Gerate GmbH (Berlin) has 4 FDA 510(k) cleared medical devices. Based in Berlin, DE.
Historical record: 4 cleared submissions from 2003 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mgb Endoskopische Gerate GmbH (Berlin) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mgb Endoskopische Gerate GmbH (Berlin)
4 devices