Sysmex Corporation of America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sysmex Corporation of America - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Sysmex Corporation of America has 3 FDA 510(k) cleared medical devices. Based in Long Grove, US.
Historical record: 3 cleared submissions from 2000 to 2002. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Sysmex Corporation of America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sysmex Corporation of America
3 devices