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FDA 510(k)

BD FlowSmart Set/MiniMed Pro-Set

K-Number: K181718 · 2018-10-18

ApplicantBecton, Dickinson and Company
Decision Date2018-10-18
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD FlowSmart Set/MiniMed Pro-Set is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2018-10-18 under approval number K181718. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD FlowSmart Set/MiniMed Pro-Set?

BD FlowSmart Set/MiniMed Pro-Set is a medical device that received FDA 510(k) clearance on 2018-10-18. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K181718.

When was BD FlowSmart Set/MiniMed Pro-Set approved by the FDA?

BD FlowSmart Set/MiniMed Pro-Set received FDA 510(k) clearance on 2018-10-18, under approval number K181718.

What company makes BD FlowSmart Set/MiniMed Pro-Set?

BD FlowSmart Set/MiniMed Pro-Set is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD FlowSmart Set/MiniMed Pro-Set?

The FDA product code for BD FlowSmart Set/MiniMed Pro-Set is FPA.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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