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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