FDA 510(k)

I.V. Administration Set

K-Number: K242126 · 2024-08-22

Decision Date2024-08-22

Product CodeFPA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

I.V. Administration Set is a medical device manufactured by Bq Plus Medical Co., Ltd.. It received FDA 510(k) clearance on 2024-08-22 under approval number K242126. 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. Administration Set is a medical device that received FDA 510(k) clearance on 2024-08-22. It is manufactured by Bq Plus Medical Co., Ltd.. The 510(k) number is K242126.

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

I.V. Administration Set received FDA 510(k) clearance on 2024-08-22, under approval number K242126.

What company makes I.V. Administration Set?

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

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

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

Other Devices by Bq Plus Medical Co., Ltd.

K210381I.V. Administration Set K223645I.V. Administration Set, I.V. Extension Set

Related Devices (Code: FPA)

K160007Paclitaxel SetsBaxter Healthcare Corporation K162304Q2 Multiport IV Administration Sets and Extension Sets, Checkmate Multiport IV Administration Sets, Q2 Extension SetsQuest Medical, Inc. K161323Solution Set for Epidural UseBaxter Healthcare Corporation K153731LifeFlow Rapid Infusion Device (LifeFlow Device)410 Medical Innovation, LLC K153440PowerLoc MAX Power Injectable Infusion Set, SafeStep Huber Needle SetC.R. Bard, Inc. K160648MiniMed Quick-Set® MiniMed Sure-T® MiniMed Silhouette® MiniMed Mio®Unomedical A/S

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.