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FDA 510(k) Applications Submitted by R-Biopharm AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171511
05/24/2017
RIDA GENE Norovirus GI/GII
R-Biopharm AG
DEN110001
02/16/2011
RIDASCREEN NOROVIRUS 3RD GENERATION EIA
R-Biopharm AG
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