FDA 510(k) Applications Submitted by BIEGLER GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K152571 09/09/2015 Stivax BIEGLER GMBH
K140788 03/31/2014 P-STIM BIEGLER GMBH
K121198 04/19/2012 BW685, BW685S BIEGLER GMBH


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