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FDA 510(k)

CLAROX

K-Number: K221286 · 2022-06-29

ApplicantVsi Co., Ltd.
Decision Date2022-06-29
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLAROX is a medical device manufactured by Vsi Co., Ltd.. It received FDA 510(k) clearance on 2022-06-29 under approval number K221286. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAROX?

CLAROX is a medical device that received FDA 510(k) clearance on 2022-06-29. It is manufactured by Vsi Co., Ltd.. The 510(k) number is K221286.

When was CLAROX approved by the FDA?

CLAROX received FDA 510(k) clearance on 2022-06-29, under approval number K221286.

What company makes CLAROX?

CLAROX is manufactured by Vsi Co., Ltd..

What is the FDA product code for CLAROX?

The FDA product code for CLAROX is EHD.

Other Devices by Vsi Co., Ltd.

K221417CLAROX plus (Model: VX-100)

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Official Source

View on FDA Database →

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

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