FDA 510(k)

Infusion Sets for Single Use

Numéro K : K202437 · 2022-03-25

DemandeurJiangsu Suyun Medical Materials Co., Ltd.

Date de décision2022-03-25

Code produitFPA

Comité consultatifHO

DécisionSubstantially Equivalent

Résumé du dispositif

Infusion Sets for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Suyun Medical Materials Co., Ltd.. It received FDA 510(k) clearance on 2022-03-25 under 510(k) number K202437. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

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. The listed applicant is Jiangsu Suyun Medical Materials Co., Ltd.. The 510(k) number is K202437.

When did Infusion Sets for Single Use receive FDA 510(k) clearance?

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

Who is the listed applicant for Infusion Sets for Single Use?

The FDA 510(k) record lists Jiangsu Suyun Medical Materials Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

Essais cliniques associés

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Dispositifs connexes (Code : FPA)

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Source officielle

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