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FDA 510(k)

Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro

N.º K: K250067 · 2025-02-20

SolicitanteGuangzhou Decheng Biotechnology Co., Ltd.
Fecha de decisión2025-02-20
Código de productoNGL
Comité asesorTX
DecisiónSubstantially Equivalent

Resumen del dispositivo

Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Decheng Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2025-02-20 under 510(k) number K250067. The device is classified under product code NGL. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro?

Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro is a medical device that received FDA 510(k) clearance on 2025-02-20. The listed applicant is Guangzhou Decheng Biotechnology Co., Ltd.. The 510(k) number is K250067.

When did Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro receive FDA 510(k) clearance?

Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro received FDA 510(k) clearance on 2025-02-20, under 510(k) number K250067.

Who is the listed applicant for Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro?

The FDA 510(k) record lists Guangzhou Decheng Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro?

The FDA product code for Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro is NGL.

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Dispositivos relacionados (Código: NGL)

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.

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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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