Medi USA, LP - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Medi USA, LP has 4 FDA 510(k) cleared medical devices. Based in Arlington Heights, US.
Last cleared in 2022. Active since 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medi USA, LP Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medi USA, LP
4 devices
Cleared
Jul 07, 2022
medi pneumatic compression system (pcs)-genius (Model 652)
Cardiovascular
30d
Cleared
Jan 25, 2019
medi pneumatic compression system (pcs) – brio (Model 651)
Cardiovascular
30d
Cleared
Dec 05, 2005
MEDI BUTLER
General Hospital
199d
Cleared
Jun 15, 1994
MEDI STRUMPF
General Hospital
56d