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FDA 510(k) Applications Submitted by GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191957
07/23/2019
BD MAX Vaginal Panel
GeneOhm Sciences Canada, Inc. (BD Diagnostics)
K130470
02/25/2013
BD MAX CDIFF ASSAY, BD MAX INSTRUMENT
GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)
K132822
09/09/2013
BD MAX STAPHSR ASSAY, INSTRUMENT
GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)
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