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FDA 510(k) Applications Submitted by M.TH. PLAUMANN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090817
03/25/2009
IONOLUX
VOCO GMBH
K113563
11/21/2011
N-HYBRIDE-COMPOSITE LC
VOCO GMBH
K143486
12/08/2014
Ufi Gel hard C
VOCO GMBH
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