FDA 510(k) Applications Submitted by PreAnalytiX GmbH

FDA 510(k) Number Submission Date Device Name Applicant
K231469 05/22/2023 PAXgene« Blood DNA Tube PreAnalytiX GmbH
DEN050003 02/28/2005 PAXGENE BLOOD RNA SYSTEM PREANALYTIX GMBH
K142821 09/30/2014 PAXgene Blood DNA Tube PREANALYTIX GMBH
K082150 07/30/2008 MODIFICATION TO PAXGENE BLOOD RNA SYSTEM PREANALYTIX GMBH


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