FDA 510(k)

Extension tube

Número K: K251788 · 2026-03-05

RequerenteZhuhai DR Medical Instruments Co., Ltd.

Data da decisão2026-03-05

Código do produtoDXT

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Extension tube is the device name listed in this FDA 510(k) record. The listed applicant is Zhuhai DR Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2026-03-05 under 510(k) number K251788. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Extension tube?

Extension tube is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Zhuhai DR Medical Instruments Co., Ltd.. The 510(k) number is K251788.

When did Extension tube receive FDA 510(k) clearance?

Extension tube received FDA 510(k) clearance on 2026-03-05, under 510(k) number K251788.

Who is the listed applicant for Extension tube?

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

What is the FDA product code for Extension tube?

The FDA product code for Extension tube is DXT.

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Fonte oficial

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