Eclipse DermaFlex 管针
K号: K200017 · 2020-11-05
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器械摘要
常见问题
What is the Eclipse DermaFlex Cannula?
Eclipse DermaFlex Cannula is a medical device that received FDA 510(k) clearance on 2020-11-05. The listed applicant is Eclipse Medcorp, LLC. The 510(k) number is K200017.
When did Eclipse DermaFlex Cannula receive FDA 510(k) clearance?
Eclipse DermaFlex Cannula received FDA 510(k) clearance on 2020-11-05, under 510(k) number K200017.
Who is the listed applicant for Eclipse DermaFlex Cannula?
The FDA 510(k) record lists Eclipse Medcorp, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Eclipse DermaFlex Cannula?
The FDA product code for Eclipse DermaFlex Cannula is FMI.
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Eclipse Medcorp, LLC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:FMI)
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。
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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