FDA 510(k)

Single Use Grasping Forceps

Número K: K191900 · 2020-03-27

RequerenteZhejiang Chuangxiang Medical Technology Co., Ltd.

Data da decisão2020-03-27

Código do produtoOCZ

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Single Use Grasping Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-03-27 under 510(k) number K191900. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Single Use Grasping Forceps?

Single Use Grasping Forceps is a medical device that received FDA 510(k) clearance on 2020-03-27. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. The 510(k) number is K191900.

When did Single Use Grasping Forceps receive FDA 510(k) clearance?

Single Use Grasping Forceps received FDA 510(k) clearance on 2020-03-27, under 510(k) number K191900.

Who is the listed applicant for Single Use Grasping Forceps?

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

What is the FDA product code for Single Use Grasping Forceps?

The FDA product code for Single Use Grasping Forceps is OCZ.

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Fonte oficial

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