FDA 510(k)

CLAROX plus (Model: VX-100)

K-Number: K221417 · 2022-09-13

Decision Date2022-09-13

Product CodeIZL

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CLAROX plus (Model: VX-100) is a medical device manufactured by Vsi Co., Ltd.. It received FDA 510(k) clearance on 2022-09-13 under approval number K221417. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAROX plus (Model: VX-100)?

CLAROX plus (Model: VX-100) is a medical device that received FDA 510(k) clearance on 2022-09-13. It is manufactured by Vsi Co., Ltd.. The 510(k) number is K221417.

When was CLAROX plus (Model: VX-100) approved by the FDA?

CLAROX plus (Model: VX-100) received FDA 510(k) clearance on 2022-09-13, under approval number K221417.

What company makes CLAROX plus (Model: VX-100)?

CLAROX plus (Model: VX-100) is manufactured by Vsi Co., Ltd..

What is the FDA product code for CLAROX plus (Model: VX-100)?

The FDA product code for CLAROX plus (Model: VX-100) is IZL.

Other Devices by Vsi Co., Ltd.

K221286CLAROX

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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.