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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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