FDA 510(k)

Red Wave Hair Removal

Número K: K212099 · 2021-09-24

RequerenteShenzhen Accompany Technology Co., Ltd.

Data da decisão2021-09-24

Código do produtoONF

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Red Wave Hair Removal is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Accompany Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-09-24 under 510(k) number K212099. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Red Wave Hair Removal?

Red Wave Hair Removal is a medical device that received FDA 510(k) clearance on 2021-09-24. The listed applicant is Shenzhen Accompany Technology Co., Ltd.. The 510(k) number is K212099.

When did Red Wave Hair Removal receive FDA 510(k) clearance?

Red Wave Hair Removal received FDA 510(k) clearance on 2021-09-24, under 510(k) number K212099.

Who is the listed applicant for Red Wave Hair Removal?

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

What is the FDA product code for Red Wave Hair Removal?

The FDA product code for Red Wave Hair Removal is ONF.

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