FDA 510(k)

Disposable Endoscopic Hemoclip

Número K: K222146 · 2023-03-28

RequerenteJiangsu Vedkang Medical Science and Technology Co., Ltd.

Data da decisão2023-03-28

Código do produtoPKL

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Disposable Endoscopic Hemoclip is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Vedkang Medical Science and Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-03-28 under 510(k) number K222146. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Disposable Endoscopic Hemoclip?

Disposable Endoscopic Hemoclip is a medical device that received FDA 510(k) clearance on 2023-03-28. The listed applicant is Jiangsu Vedkang Medical Science and Technology Co., Ltd.. The 510(k) number is K222146.

When did Disposable Endoscopic Hemoclip receive FDA 510(k) clearance?

Disposable Endoscopic Hemoclip received FDA 510(k) clearance on 2023-03-28, under 510(k) number K222146.

Who is the listed applicant for Disposable Endoscopic Hemoclip?

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

What is the FDA product code for Disposable Endoscopic Hemoclip?

The FDA product code for Disposable Endoscopic Hemoclip is PKL.

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Fonte oficial

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