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Medi USA, LP

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221654medi pneumatic compression system (pcs)-genius (Model 652)July 7, 2022
K183631medi pneumatic compression system (pcs) – brio (Model 651)January 25, 2019
K051324MEDI BUTLERDecember 5, 2005
K941926MEDI STRUMPFJune 15, 1994