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FDA 510(k)

Razor, Everest, U&C Liquid

K-Number: K191902 · 2019-10-11

ApplicantU&C International Co., Ltd.
Decision Date2019-10-11
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by U&C International Co., Ltd.. The 510(k) number is K191902.

When was Razor, Everest, U&C Liquid approved by the FDA?

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

What company makes Razor, Everest, U&C Liquid?

Razor, Everest, U&C Liquid is manufactured by U&C International Co., Ltd..

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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