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FDA 510(k)

BD Secondary Infusion Set

K-Number: K223101 · 2023-05-12

ApplicantCare Fusion
Decision Date2023-05-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD Secondary Infusion Set is a medical device manufactured by Care Fusion. It received FDA 510(k) clearance on 2023-05-12 under approval number K223101. 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 Secondary Infusion Set?

BD Secondary Infusion Set is a medical device that received FDA 510(k) clearance on 2023-05-12. It is manufactured by Care Fusion. The 510(k) number is K223101.

When was BD Secondary Infusion Set approved by the FDA?

BD Secondary Infusion Set received FDA 510(k) clearance on 2023-05-12, under approval number K223101.

What company makes BD Secondary Infusion Set?

BD Secondary Infusion Set is manufactured by Care Fusion.

What is the FDA product code for BD Secondary Infusion Set?

The FDA product code for BD Secondary Infusion 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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