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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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