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Geneohm Sciences Canada, Inc. (Bd Diagnostics)

FDA Regulatory Profile

Geneohm Sciences Canada, Inc. (Bd Diagnostics) appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 21, 2019.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K191957BD MAX Vaginal PanelOctober 21, 2019
DEN160001BD MAX Vaginal Panel, BD MAX InstrumentOctober 28, 2016
K132822BD MAX STAPHSR ASSAY, INSTRUMENTNovember 26, 2013
K130470BD MAX CDIFF ASSAY, BD MAX INSTRUMENTApril 2, 2013

FDA data resources