Fresenius AG is one of 7997 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fresenius AG - FDA 510(k) Cleared Devices
Recent clearances: C.A.T.S CONTINUOUS AUTOTRANSFUSION SYSTEM, AT1 AUTOTRANSFUSION SET, PSQ SET
2
Total
2
Cleared
0
Denied
Fresenius AG has 2 FDA 510(k) cleared medical devices. Based in Foster, US.
Historical record: 2 cleared submissions from 1996 to 1997. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Fresenius AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fresenius AG
2 devices