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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 the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Kaiyan Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2023-12-13 under 510(k) 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. The listed applicant is Shenzhen Kaiyan Medical Equipment Co., Ltd.. The 510(k) number is K232863.

When did Radiant Renewal Skincare Wand (HD-15, HD-15A) receive FDA 510(k) clearance?

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

Who is the listed applicant for Radiant Renewal Skincare Wand (HD-15, HD-15A)?

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

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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