FDA 510(k)

Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)

Numéro K : K242151 · 2025-04-08

DemandeurShenzhen Nuon Medical Equipment Co., Ltd.

Date de décision2025-04-08

Code produitOHS

Comité consultatifSU

DécisionSubstantially Equivalent

Résumé du dispositif

Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Nuon Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2025-04-08 under 510(k) number K242151. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)?

Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B) is a medical device that received FDA 510(k) clearance on 2025-04-08. The listed applicant is Shenzhen Nuon Medical Equipment Co., Ltd.. The 510(k) number is K242151.

When did Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B) receive FDA 510(k) clearance?

Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B) received FDA 510(k) clearance on 2025-04-08, under 510(k) number K242151.

Who is the listed applicant for Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)?

The FDA 510(k) record lists Shenzhen Nuon 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-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)?

The FDA product code for Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B) is OHS.

Essais cliniques associés

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Source officielle

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