FDA 510(k)

Razor, Everest, U&C Liquid

Número K: K191902 · 2019-10-11

Data da decisão2019-10-11

Código do produtoEIH

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Razor, Everest, U&C Liquid is the device name listed in this FDA 510(k) record. The listed applicant is U&C International Co., Ltd.. It received FDA 510(k) clearance on 2019-10-11 under 510(k) number K191902. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Razor, Everest, U&C Liquid?

Razor, Everest, U&C Liquid is a medical device that received FDA 510(k) clearance on 2019-10-11. The listed applicant is U&C International Co., Ltd.. The 510(k) number is K191902.

When did Razor, Everest, U&C Liquid receive FDA 510(k) clearance?

Razor, Everest, U&C Liquid received FDA 510(k) clearance on 2019-10-11, under 510(k) number K191902.

Who is the listed applicant for Razor, Everest, U&C Liquid?

The FDA 510(k) record lists U&C International Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Razor, Everest, U&C Liquid?

The FDA product code for Razor, Everest, U&C Liquid is EIH.

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