iPulse SmoothSkin BARE 毛发去除设备
K号: K163552 · 2017-03-03
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器械摘要
iPulse SmoothSkin BARE Hair Removal Device is the device name listed in this FDA 510(k) record. The listed applicant is Cyden Limited. It received FDA 510(k) clearance on 2017-03-03 under 510(k) number K163552. 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 iPulse SmoothSkin BARE Hair Removal Device?
iPulse SmoothSkin BARE Hair Removal Device is a medical device that received FDA 510(k) clearance on 2017-03-03. The listed applicant is Cyden Limited. The 510(k) number is K163552.
When did iPulse SmoothSkin BARE Hair Removal Device receive FDA 510(k) clearance?
iPulse SmoothSkin BARE Hair Removal Device received FDA 510(k) clearance on 2017-03-03, under 510(k) number K163552.
Who is the listed applicant for iPulse SmoothSkin BARE Hair Removal Device?
FDA 510(k)记录显示Cyden Limited为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for iPulse SmoothSkin BARE Hair Removal Device?
The FDA product code for iPulse SmoothSkin BARE 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Cyden Limited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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