FDA 510(k) Applications Submitted by LEVO AG

FDA 510(k) Number Submission Date Device Name Applicant
K051387 05/27/2005 LEVO COMFORT II LEVO AG
K140706 03/21/2014 LEVO MAX LEVO AG
K083017 10/09/2008 LEVO C3 LEVO AG
K030893 03/21/2003 LEVO COMBI LEVO AG


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