FDA 510(k)

Nitrile Glove

Número K: K211252 · 2021-06-25

RequerenteJiangsu Dihong Industry and Trade Co., Ltd.

Data da decisão2021-06-25

Código do produtoLZA

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Nitrile Glove is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Dihong Industry and Trade Co., Ltd.. It received FDA 510(k) clearance on 2021-06-25 under 510(k) number K211252. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Nitrile Glove?

Nitrile Glove is a medical device that received FDA 510(k) clearance on 2021-06-25. The listed applicant is Jiangsu Dihong Industry and Trade Co., Ltd.. The 510(k) number is K211252.

When did Nitrile Glove receive FDA 510(k) clearance?

Nitrile Glove received FDA 510(k) clearance on 2021-06-25, under 510(k) number K211252.

Who is the listed applicant for Nitrile Glove?

The FDA 510(k) record lists Jiangsu Dihong Industry and Trade Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nitrile Glove?

The FDA product code for Nitrile Glove is LZA.

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Outros registros que listam Jiangsu Dihong Industry and Trade Co., Ltd. como candidato(a)

K211904Vinyl Glove

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Fonte oficial

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