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BD MAX Vaginal Panel, BD MAX Instrument

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN160001
510(k) Type
Direct
Applicant
GENEOHM SCIENCES CANADA , INC (BD DIAGNOSTICS)
Country
Canada
FDA Decision
Deleted
Decision Date
10/28/2016
Days to Decision
291 days

BD MAX Vaginal Panel, BD MAX Instrument

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN160001
510(k) Type
Direct
Applicant
GENEOHM SCIENCES CANADA , INC (BD DIAGNOSTICS)
Country
Canada
FDA Decision
Deleted
Decision Date
10/28/2016
Days to Decision
291 days