Braun Silk.expert Mini
K号: K211994 · 2021-07-28
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器械摘要
Braun Silk.expert Mini is the device name listed in this FDA 510(k) record. The listed applicant is Cyden Limited. It received FDA 510(k) clearance on 2021-07-28 under 510(k) number K211994. 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 Braun Silk.expert Mini?
Braun Silk.expert Mini is a medical device that received FDA 510(k) clearance on 2021-07-28. The listed applicant is Cyden Limited. The 510(k) number is K211994.
When did Braun Silk.expert Mini receive FDA 510(k) clearance?
Braun Silk.expert Mini received FDA 510(k) clearance on 2021-07-28, under 510(k) number K211994.
Who is the listed applicant for Braun Silk.expert Mini?
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 Braun Silk.expert Mini?
The FDA product code for Braun Silk.expert Mini 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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