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FDA 510(k)

Infusion Sets for Single Use

K-Number: K202437 · 2022-03-25

Decision Date2022-03-25
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Infusion Sets for Single Use is a medical device manufactured by Jiangsu Suyun Medical Materials Co., Ltd.. It received FDA 510(k) clearance on 2022-03-25 under approval number K202437. 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 Infusion Sets for Single Use?

Infusion Sets for Single Use is a medical device that received FDA 510(k) clearance on 2022-03-25. It is manufactured by Jiangsu Suyun Medical Materials Co., Ltd.. The 510(k) number is K202437.

When was Infusion Sets for Single Use approved by the FDA?

Infusion Sets for Single Use received FDA 510(k) clearance on 2022-03-25, under approval number K202437.

What company makes Infusion Sets for Single Use?

Infusion Sets for Single Use is manufactured by Jiangsu Suyun Medical Materials Co., Ltd..

What is the FDA product code for Infusion Sets for Single Use?

The FDA product code for Infusion Sets for Single Use is FPA.

Related Clinical Trials

Related Devices (Code: FPA)

Official Source

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