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BD MAX CT/GC/TV, BD MAX INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151589
510(k) Type
Traditional
Applicant
BECTON, DICKINSON, AND COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2016
Days to Decision
452 days
Submission Type
Summary

BD MAX CT/GC/TV, BD MAX INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151589
510(k) Type
Traditional
Applicant
BECTON, DICKINSON, AND COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2016
Days to Decision
452 days
Submission Type
Summary