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FDA 510(k)

Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs

N.º K: K220491 · 2022-05-14

Fecha de decisión2022-05-14
Código de productoLZC
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs is the device name listed in this FDA 510(k) record. The listed applicant is Hainan Asther Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2022-05-14 under 510(k) number K220491. The device is classified under product code LZC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs?

Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs is a medical device that received FDA 510(k) clearance on 2022-05-14. The listed applicant is Hainan Asther Medical Equipment Co., Ltd.. The 510(k) number is K220491.

When did Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs receive FDA 510(k) clearance?

Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs received FDA 510(k) clearance on 2022-05-14, under 510(k) number K220491.

Who is the listed applicant for Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs?

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

What is the FDA product code for Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs?

The FDA product code for Disposable Medical Nitrile Examination Gloves -Tested for Use with Chemotherapy Drugs is LZC.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

Dispositivos relacionados (Código: LZC)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

Fuente oficial

Ver en la base de datos de la FDA →

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

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