FDA 510(k)

Denudation Pipettes

Número K: K250838 · 2025-07-03

RequerenteGuangzhou Pinzhi Medical Device Co., Ltd.

Data da decisão2025-07-03

Código do produtoMQH

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

Denudation Pipettes is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Pinzhi Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2025-07-03 under 510(k) number K250838. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Denudation Pipettes?

Denudation Pipettes is a medical device that received FDA 510(k) clearance on 2025-07-03. The listed applicant is Guangzhou Pinzhi Medical Device Co., Ltd.. The 510(k) number is K250838.

When did Denudation Pipettes receive FDA 510(k) clearance?

Denudation Pipettes received FDA 510(k) clearance on 2025-07-03, under 510(k) number K250838.

Who is the listed applicant for Denudation Pipettes?

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

What is the FDA product code for Denudation Pipettes?

The FDA product code for Denudation Pipettes is MQH.

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Fonte oficial

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