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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
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