IPL脱毛仪
K号: K222316 · 2022-09-28
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决定日期2022-09-28
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。
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器械摘要
IPL Hair Removal Device is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Goodwind Technology Development Co., Ltd.. It received FDA 510(k) clearance on 2022-09-28 under 510(k) number K222316. 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 IPL Hair Removal Device?
IPL Hair Removal Device is a medical device that received FDA 510(k) clearance on 2022-09-28. The listed applicant is Shenzhen Goodwind Technology Development Co., Ltd.. The 510(k) number is K222316.
When did IPL Hair Removal Device receive FDA 510(k) clearance?
IPL Hair Removal Device received FDA 510(k) clearance on 2022-09-28, under 510(k) number K222316.
Who is the listed applicant for IPL Hair Removal Device?
FDA 510(k)记录将深圳好风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 IPL Hair Removal Device?
The FDA product code for IPL 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 Goodwind Technology Development 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。
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。
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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