FDA 510(k)

IPL Home Use Hair Removal Device

Número K: K211922 · 2021-09-20

RequerenteShenzhen Beauty Every Moment Intelligent Electric Co., Ltd.

Data da decisão2021-09-20

Código do produtoOHT

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

IPL Home Use Hair Removal Device is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.. It received FDA 510(k) clearance on 2021-09-20 under 510(k) number K211922. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the IPL Home Use Hair Removal Device?

IPL Home Use Hair Removal Device is a medical device that received FDA 510(k) clearance on 2021-09-20. The listed applicant is Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.. The 510(k) number is K211922.

When did IPL Home Use Hair Removal Device receive FDA 510(k) clearance?

IPL Home Use Hair Removal Device received FDA 510(k) clearance on 2021-09-20, under 510(k) number K211922.

Who is the listed applicant for IPL Home Use Hair Removal Device?

The FDA 510(k) record lists Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPL Home Use Hair Removal Device?

The FDA product code for IPL Home Use Hair Removal Device is OHT.

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Outros registros que listam Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. como candidato(a)

K240583IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)K221001IPL Home Use Hair Removal Device K211185IPL Home Use Hair Removal Device

Dispositivos Relacionados (Código: OHT)

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