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BD SmartSite™ 13mm Vial Access Device; BD SmartSite™ 20mm Vial Access Device

Page Type
Cleared 510(K)
510(k) Number
K233021
510(k) Type
Traditional
Applicant
CareFusion
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2024
Days to Decision
166 days
Submission Type
Summary

BD SmartSite™ 13mm Vial Access Device; BD SmartSite™ 20mm Vial Access Device

Page Type
Cleared 510(K)
510(k) Number
K233021
510(k) Type
Traditional
Applicant
CareFusion
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2024
Days to Decision
166 days
Submission Type
Summary