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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 the device name listed in this FDA 510(k) record. The listed applicant is Vsi Co., Ltd.. It received FDA 510(k) clearance on 2022-06-29 under 510(k) 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. The listed applicant is Vsi Co., Ltd.. The 510(k) number is K221286.

When did CLAROX receive FDA 510(k) clearance?

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

Who is the listed applicant for CLAROX?

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

What is the FDA product code for CLAROX?

The FDA product code for CLAROX is EHD.

Other records listing Vsi Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K221417CLAROX plus (Model: VX-100)

Related Devices (Code: EHD)

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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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