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FDA 510(k) Applications Submitted by MEDI USA, LP
FDA 510(k) Number
Submission Date
Device Name
Applicant
K051324
05/20/2005
MEDI BUTLER
MEDI USA, LP
K183631
12/26/2018
medi pneumatic compression system (pcs) û brio (Model 651)
Medi USA, LP
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