FDA 510(k)

Vent Vial Adapter

Número K: K233287 · 2024-07-26

RequerenteHangzhou Qiantang Longyue Biotechnology Co., Ltd.

Data da decisão2024-07-26

Código do produtoLHI

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vent Vial Adapter is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2024-07-26 under 510(k) number K233287. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Vent Vial Adapter?

Vent Vial Adapter is a medical device that received FDA 510(k) clearance on 2024-07-26. The listed applicant is Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. The 510(k) number is K233287.

When did Vent Vial Adapter receive FDA 510(k) clearance?

Vent Vial Adapter received FDA 510(k) clearance on 2024-07-26, under 510(k) number K233287.

Who is the listed applicant for Vent Vial Adapter?

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

What is the FDA product code for Vent Vial Adapter?

The FDA product code for Vent Vial Adapter is LHI.

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Outros registros que listam Hangzhou Qiantang Longyue Biotechnology Co., Ltd. como candidato(a)

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Dispositivos Relacionados (Código: LHI)

K252987ADRx® Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LP K251715FlowArt® Vial Access Device VentedAsset Medikal K251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLC K243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

Fonte oficial

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