Fresenius Hemotechnology, Inc. is one of 7959 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fresenius Hemotechnology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FRESENIUS ATR40 AND ATR120 AUTOTRANSFUSION RESERVOIRS, C.A.T.S AUTOTRANSFUSION ACCESSORIES, MODELS ATS SUCTION LINE, ATY Y-ADAPTER, AND ATO OXYGENATOR LINE
3
Total
3
Cleared
0
Denied
Fresenius Hemotechnology, Inc. has 3 FDA 510(k) cleared medical devices. Based in Redmond, US.
Historical record: 3 cleared submissions from 1999 to 2001. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Fresenius Hemotechnology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fresenius Hemotechnology, Inc.
3 devices