FDA 510(k)

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

K号: K221643 · 2022-10-21

决定日期2022-10-21

产品代码OHT

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决定实质等同

器械摘要

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.

常见问题

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.

列明Shenzhen Desida Technology Co., Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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