FDA 510(k)

Sterile hypodermic syringes for single use

Numéro K : K211728 · 2021-10-05

DemandeurJiangsu Kangyou Medical Instrument Co., Ltd.

Date de décision2021-10-05

Code produitFMF

Comité consultatifHO

DécisionSubstantially Equivalent

Résumé du dispositif

Sterile hypodermic syringes for single use is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Kangyou Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2021-10-05 under 510(k) number K211728. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Sterile hypodermic syringes for single use?

Sterile hypodermic syringes for single use is a medical device that received FDA 510(k) clearance on 2021-10-05. The listed applicant is Jiangsu Kangyou Medical Instrument Co., Ltd.. The 510(k) number is K211728.

When did Sterile hypodermic syringes for single use receive FDA 510(k) clearance?

Sterile hypodermic syringes for single use received FDA 510(k) clearance on 2021-10-05, under 510(k) number K211728.

Who is the listed applicant for Sterile hypodermic syringes for single use?

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

What is the FDA product code for Sterile hypodermic syringes for single use?

The FDA product code for Sterile hypodermic syringes for single use is FMF.

Essais cliniques associés

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Dispositifs connexes (Code : FMF)

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Source officielle

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