FDA 510(k)

Victan

N.º K: K230593 · 2023-05-30

SolicitanteJiangsu Haize Medical Scientific Development Co., Ltd.

Fecha de decisión2023-05-30

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Victan is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Haize Medical Scientific Development Co., Ltd.. It received FDA 510(k) clearance on 2023-05-30 under 510(k) number K230593. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Victan?

Victan is a medical device that received FDA 510(k) clearance on 2023-05-30. The listed applicant is Jiangsu Haize Medical Scientific Development Co., Ltd.. The 510(k) number is K230593.

When did Victan receive FDA 510(k) clearance?

Victan received FDA 510(k) clearance on 2023-05-30, under 510(k) number K230593.

Who is the listed applicant for Victan?

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

What is the FDA product code for Victan?

The FDA product code for Victan is GEI.

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Fuente oficial

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