FDA 510(k)

Nitrile Glove

N.º K: K211252 · 2021-06-25

SolicitanteJiangsu Dihong Industry and Trade Co., Ltd.

Fecha de decisión2021-06-25

Código de productoLZA

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del 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.

Preguntas frecuentes

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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Otros registros que enlistan a Jiangsu Dihong Industry and Trade Co., Ltd. como solicitante

K211904Vinyl Glove

Dispositivos relacionados (Código: LZA)

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Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.