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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