Geneohm Sciences Canada, Inc. (BD Diagnostics)
CanadaFDA applicant, unverified
- Devices
- 4
Catalogue
BD MAX Vaginal Panel Ref K191957
Regimes: 510(k) Registry: 510(k)BD MAX Vaginal Panel, BD MAX Instrument Ref DEN160001
Regimes: De Novo Registry: De NovoBd Max Cdiff Assay, Bd Max Instrument Ref K130470
Regimes: 510(k) Registry: 510(k)Bd Max Staphsr Assay, Instrument Ref K132822
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geneohm Sciences Canada, Inc. (Bd Diagnostics) have in the registry?
The registry currently lists 4 devices for Geneohm Sciences Canada, Inc. (Bd Diagnostics). Devices recorded under merged duplicate company entries are counted once.
Which registries list Geneohm Sciences Canada, Inc. (Bd Diagnostics)'s devices?
Among its 4 most recently registered devices, Geneohm Sciences Canada, Inc. (Bd Diagnostics) has devices listed in FDA 510(k) (4 devices).
What risk classes do Geneohm Sciences Canada, Inc. (Bd Diagnostics)'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Geneohm Sciences Canada, Inc. (Bd Diagnostics)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geneohm Sciences Canada, Inc. (Bd Diagnostics) in the registry?
The most recently registered devices listed for Geneohm Sciences Canada, Inc. (Bd Diagnostics) include BD MAX Vaginal Panel, BD MAX Vaginal Panel, BD MAX Instrument, BD MAX CDIFF ASSAY, BD MAX INSTRUMENT and BD MAX STAPHSR ASSAY, INSTRUMENT.