FDA 510(k)

Hair Removal Device (Model: IPL-D26, IPL-D19)

Número K: K221643 · 2022-10-21

RequerenteShenzhen Desida Technology Co., Ltd.

Data da decisão2022-10-21

Código do produtoOHT

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Hair Removal Device (Model: IPL-D26, IPL-D19) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Desida Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-10-21 under 510(k) number K221643. 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 Hair Removal Device (Model: IPL-D26, IPL-D19)?

Hair Removal Device (Model: IPL-D26, IPL-D19) is a medical device that received FDA 510(k) clearance on 2022-10-21. The listed applicant is Shenzhen Desida Technology Co., Ltd.. The 510(k) number is K221643.

When did Hair Removal Device (Model: IPL-D26, IPL-D19) receive FDA 510(k) clearance?

Hair Removal Device (Model: IPL-D26, IPL-D19) received FDA 510(k) clearance on 2022-10-21, under 510(k) number K221643.

Who is the listed applicant for Hair Removal Device (Model: IPL-D26, IPL-D19)?

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

What is the FDA product code for Hair Removal Device (Model: IPL-D26, IPL-D19)?

The FDA product code for Hair Removal Device (Model: IPL-D26, IPL-D19) is OHT.

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