Geneohm Sciences Canada, Inc. (Bd Diagnostics)

Geneohm Sciences Canada, Inc. (Bd Diagnostics) holds 4 FDA 510(k) medical device clearances, first cleared 2013, most recent 2019.

Top product codes for Geneohm Sciences Canada, Inc. (Bd Diagnostics)

Recent clearances by Geneohm Sciences Canada, Inc. (Bd Diagnostics)

K191957 — BD MAX Vaginal PanelCode PQA·2019-10-21
DEN160001 — BD MAX Vaginal Panel, BD MAX InstrumentCode PQA·2016-10-28
K132822 — BD MAX STAPHSR ASSAY, INSTRUMENTCode NQX·2013-11-26
K130470 — BD MAX CDIFF ASSAY, BD MAX INSTRUMENTCode OZN·2013-04-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.