维纳斯丝质专家
K号: K170734 · 2017-05-08
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器械摘要
Venus Silk.expert is the device name listed in this FDA 510(k) record. The listed applicant is Cyden Limited. It received FDA 510(k) clearance on 2017-05-08 under 510(k) number K170734. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Venus Silk.expert?
Venus Silk.expert is a medical device that received FDA 510(k) clearance on 2017-05-08. The listed applicant is Cyden Limited. The 510(k) number is K170734.
When did Venus Silk.expert receive FDA 510(k) clearance?
Venus Silk.expert received FDA 510(k) clearance on 2017-05-08, under 510(k) number K170734.
Who is the listed applicant for Venus Silk.expert?
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 Venus Silk.expert?
The FDA product code for Venus Silk.expert is GEX. This falls under the Gastroenterology category.
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：GEX）
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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