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FDA 510(k)

手持式IPL设备(JOVS脱毛设备)

K号: K220645 · 2022-04-27

决定日期2022-04-27
产品代码OHT
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

Hand-held IPL device (JOVS Hair Removal Device) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Qianyu Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-04-27 under 510(k) number K220645. 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 Hand-held IPL device (JOVS Hair Removal Device)?

Hand-held IPL device (JOVS Hair Removal Device) is a medical device that received FDA 510(k) clearance on 2022-04-27. The listed applicant is Shenzhen Qianyu Technology Co., Ltd.. The 510(k) number is K220645.

When did Hand-held IPL device (JOVS Hair Removal Device) receive FDA 510(k) clearance?

Hand-held IPL device (JOVS Hair Removal Device) received FDA 510(k) clearance on 2022-04-27, under 510(k) number K220645.

Who is the listed applicant for Hand-held IPL device (JOVS Hair Removal Device)?

FDA 510(k)记录将深圳前域科技有限公司列为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for Hand-held IPL device (JOVS Hair Removal Device)?

The FDA product code for Hand-held IPL device (JOVS Hair Removal Device) is OHT.

相关临床试验

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。

列明Shenzhen Qianyu 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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相关器械(代码:OHT)

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。

官方来源

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