FDA 510(k)

Vericor Support Catheter

Número K: K222679 · 2022-11-07

RequerenteVascupatent Medical (Shenzhen) Co., Ltd.

Data da decisão2022-11-07

Código do produtoKRA

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vericor Support Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Vascupatent Medical (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2022-11-07 under 510(k) number K222679. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Vericor Support Catheter?

Vericor Support Catheter is a medical device that received FDA 510(k) clearance on 2022-11-07. The listed applicant is Vascupatent Medical (Shenzhen) Co., Ltd.. The 510(k) number is K222679.

When did Vericor Support Catheter receive FDA 510(k) clearance?

Vericor Support Catheter received FDA 510(k) clearance on 2022-11-07, under 510(k) number K222679.

Who is the listed applicant for Vericor Support Catheter?

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

What is the FDA product code for Vericor Support Catheter?

The FDA product code for Vericor Support Catheter is KRA.

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Fonte oficial

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