Fresenius USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FRESENIUS MODIFIED F400 LOW VOLUME HEMOCONCENTRATOR F3000 & MODIFIED F400 LOW VOL HEMOCONCENTRATOR W/TUBING SET F3000TS, FRESENIUS POLYSULFONE HEMODIALYZERS, BOTH LOW AND HIGH FLUX, FRESENIUS F SERIES HEMOCONCENTRATORS F400,F500,F700,F800,F400TS,F500TS,F700S,F800TS
38
Total
37
Cleared
0
Denied
FDA 510(k) Regulatory Record - Fresenius USA, Inc. Anesthesiology ✕
1 devices