FDA 510(k)

Disposable Endoscope Injection Needles

Número K: K232442 · 2023-11-09

RequerenteZhejiang Soudon Medical Technology Co., Ltd.

Data da decisão2023-11-09

Código do produtoFBK

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Disposable Endoscope Injection Needles is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Soudon Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-11-09 under 510(k) number K232442. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Disposable Endoscope Injection Needles?

Disposable Endoscope Injection Needles is a medical device that received FDA 510(k) clearance on 2023-11-09. The listed applicant is Zhejiang Soudon Medical Technology Co., Ltd.. The 510(k) number is K232442.

When did Disposable Endoscope Injection Needles receive FDA 510(k) clearance?

Disposable Endoscope Injection Needles received FDA 510(k) clearance on 2023-11-09, under 510(k) number K232442.

Who is the listed applicant for Disposable Endoscope Injection Needles?

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

What is the FDA product code for Disposable Endoscope Injection Needles?

The FDA product code for Disposable Endoscope Injection Needles is FBK.

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Dispositivos Relacionados (Código: FBK)

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Fonte oficial

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