BRAUN Silk.expert Pro 5
K号: K190354 · 2019-03-18
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器械摘要
BRAUN Silk.expert Pro 5 is the device name listed in this FDA 510(k) record. The listed applicant is Cyden Limited. It received FDA 510(k) clearance on 2019-03-18 under 510(k) number K190354. 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 Pro 5?
BRAUN Silk.expert Pro 5 is a medical device that received FDA 510(k) clearance on 2019-03-18. The listed applicant is Cyden Limited. The 510(k) number is K190354.
When did BRAUN Silk.expert Pro 5 receive FDA 510(k) clearance?
BRAUN Silk.expert Pro 5 received FDA 510(k) clearance on 2019-03-18, under 510(k) number K190354.
Who is the listed applicant for BRAUN Silk.expert Pro 5?
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 Pro 5?
The FDA product code for BRAUN Silk.expert Pro 5 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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