FDA 510(k)

I.V. Administration Set, I.V. Extension Set

K-Number: K223645 · 2023-05-18

Decision Date2023-05-18

Product CodeFPA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

I.V. Administration Set, I.V. Extension Set is a medical device manufactured by Bq Plus Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-05-18 under approval number K223645. 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 I.V. Administration Set, I.V. Extension Set?

I.V. Administration Set, I.V. Extension Set is a medical device that received FDA 510(k) clearance on 2023-05-18. It is manufactured by Bq Plus Medical Co., Ltd.. The 510(k) number is K223645.

When was I.V. Administration Set, I.V. Extension Set approved by the FDA?

I.V. Administration Set, I.V. Extension Set received FDA 510(k) clearance on 2023-05-18, under approval number K223645.

What company makes I.V. Administration Set, I.V. Extension Set?

I.V. Administration Set, I.V. Extension Set is manufactured by Bq Plus Medical Co., Ltd..

What is the FDA product code for I.V. Administration Set, I.V. Extension Set?

The FDA product code for I.V. Administration Set, I.V. Extension Set is FPA.

Other Devices by Bq Plus Medical Co., Ltd.

K210381I.V. Administration Set K242126I.V. Administration Set

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Official Source

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