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FDA 510(k) Applications Submitted by VOLKER JOACHIM FRIEMERT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K083842
12/24/2008
ROTEM DELTA THROMBOELASTOMETRY SYSTEM
PENTAPHARM GMBH
K101533
06/03/2010
EX-TEM. FIB-TEM, AND AP-TEM FOR ROTEM DELTA THROMBOELASTOMETRY SYSTEM
Tem Innovations GmbH
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