freeflex+ 转接适配器
K号: K212445 · 2022-06-01
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器械摘要
常见问题
What is the freeflex+ Transfer Adapter?
freeflex+ Transfer Adapter is a medical device that received FDA 510(k) clearance on 2022-06-01. The listed applicant is Fresenius Kabi AG. The 510(k) number is K212445.
When did freeflex+ Transfer Adapter receive FDA 510(k) clearance?
freeflex+ Transfer Adapter received FDA 510(k) clearance on 2022-06-01, under 510(k) number K212445.
Who is the listed applicant for freeflex+ Transfer Adapter?
The FDA 510(k) record lists Fresenius Kabi AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for freeflex+ Transfer Adapter?
The FDA product code for freeflex+ Transfer Adapter is LHI.
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Fresenius Kabi AG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:LHI)
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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