FDA 510(k)

Endofresh Digestive Endoscopy System

Número K: K192704 · 2020-09-02

RequerenteHuizhou Xzing Technology Co., Ltd.

Data da decisão2020-09-02

Código do produtoFDS

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Endofresh Digestive Endoscopy System is the device name listed in this FDA 510(k) record. The listed applicant is Huizhou Xzing Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K192704. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Endofresh Digestive Endoscopy System?

Endofresh Digestive Endoscopy System is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is Huizhou Xzing Technology Co., Ltd.. The 510(k) number is K192704.

When did Endofresh Digestive Endoscopy System receive FDA 510(k) clearance?

Endofresh Digestive Endoscopy System received FDA 510(k) clearance on 2020-09-02, under 510(k) number K192704.

Who is the listed applicant for Endofresh Digestive Endoscopy System?

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

What is the FDA product code for Endofresh Digestive Endoscopy System?

The FDA product code for Endofresh Digestive Endoscopy System is FDS.

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