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FDA 510(k) Applications Submitted by MATTHIAS WEBER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K132416
08/02/2013
REHASTIM 2, ERIGOPRO (FES)
HASOMED GMBH
K112844
09/29/2011
REHASTIM 2, REHAMOVE 2
HASOMED GMBH
K073237
11/16/2007
REHASTIM & REHAMOVE
HASOMED GMBH
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