Last synced on 14 November 2025 at 11:06 pm

BD MAX MRSA XT, BD MAX INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K133605
510(k) Type
Traditional
Applicant
GENEOHM SCIENCES CANADA, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/20/2013
Days to Decision
25 days
Submission Type
Summary

BD MAX MRSA XT, BD MAX INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K133605
510(k) Type
Traditional
Applicant
GENEOHM SCIENCES CANADA, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/20/2013
Days to Decision
25 days
Submission Type
Summary