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FDA 510(k)

Radiant Renewal Skincare Wand (HD-15, HD-15A)

K-Number: K232863 · 2023-12-13

ApplicantShenzhen Kaiyan Medical Equipment Co., Ltd.
Decision Date2023-12-13
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Radiant Renewal Skincare Wand (HD-15, HD-15A) is a medical device manufactured by Shenzhen Kaiyan Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2023-12-13 under approval number K232863. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Radiant Renewal Skincare Wand (HD-15, HD-15A)?

Radiant Renewal Skincare Wand (HD-15, HD-15A) is a medical device that received FDA 510(k) clearance on 2023-12-13. It is manufactured by Shenzhen Kaiyan Medical Equipment Co., Ltd.. The 510(k) number is K232863.

When was Radiant Renewal Skincare Wand (HD-15, HD-15A) approved by the FDA?

Radiant Renewal Skincare Wand (HD-15, HD-15A) received FDA 510(k) clearance on 2023-12-13, under approval number K232863.

What company makes Radiant Renewal Skincare Wand (HD-15, HD-15A)?

Radiant Renewal Skincare Wand (HD-15, HD-15A) is manufactured by Shenzhen Kaiyan Medical Equipment Co., Ltd..

What is the FDA product code for Radiant Renewal Skincare Wand (HD-15, HD-15A)?

The FDA product code for Radiant Renewal Skincare Wand (HD-15, HD-15A) is OHS.

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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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