FDA 510(k)

Dochek® Multi-Drug Urine Test Cup Rx, Dochek® Multi-Drug Urine Test Cup

Número K: K232659 · 2023-12-13

RequerenteGuangzhou Decheng Biotechnology Co., Ltd.

Data da decisão2023-12-13

Código do produtoDJG

Comité consultivoTX

DecisãoSubstantially Equivalent

Resumo do dispositivo

Dochek® Multi-Drug Urine Test Cup Rx, Dochek® Multi-Drug Urine Test Cup 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 2023-12-13 under 510(k) number K232659. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Dochek® Multi-Drug Urine Test Cup Rx, Dochek® Multi-Drug Urine Test Cup?

Dochek® Multi-Drug Urine Test Cup Rx, Dochek® Multi-Drug Urine Test Cup is a medical device that received FDA 510(k) clearance on 2023-12-13. The listed applicant is Guangzhou Decheng Biotechnology Co., Ltd.. The 510(k) number is K232659.

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

Dochek® Multi-Drug Urine Test Cup Rx, Dochek® Multi-Drug Urine Test Cup received FDA 510(k) clearance on 2023-12-13, under 510(k) number K232659.

Who is the listed applicant for Dochek® Multi-Drug Urine Test Cup Rx, Dochek® Multi-Drug Urine Test Cup?

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 Rx, Dochek® Multi-Drug Urine Test Cup?

The FDA product code for Dochek® Multi-Drug Urine Test Cup Rx, Dochek® Multi-Drug Urine Test Cup is DJG.

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Outros registros que listam Guangzhou Decheng Biotechnology Co., Ltd. como candidato(a)

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Fonte oficial

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