FDA 510(k)

Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)

K-Nummer: K251034 · 2025-10-12

AntragstellerShenzhen Nuon Medical Equipment Co., Ltd.

Entscheidungsdatum2025-10-12

ProduktcodeNFO

BeratungsausschussNE

EntscheidungSubstantially Equivalent

Produktübersicht

Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) 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 2025-10-12 under 510(k) number K251034. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)?

Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) is a medical device that received FDA 510(k) clearance on 2025-10-12. The listed applicant is Shenzhen Nuon Medical Equipment Co., Ltd.. The 510(k) number is K251034.

When did Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) receive FDA 510(k) clearance?

Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) received FDA 510(k) clearance on 2025-10-12, under 510(k) number K251034.

Who is the listed applicant for Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)?

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 Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)?

The FDA product code for Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) is NFO.

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Weitere Einträge mit Shenzhen Nuon Medical Equipment Co., Ltd. als Antragsteller

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