BD FlowSmart Set, MiniMed Pro-Set
K号: K160651 · 2016-04-07
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器械摘要
常见问题
What is the BD FlowSmart Set, MiniMed Pro-Set?
BD FlowSmart Set, MiniMed Pro-Set is a medical device that received FDA 510(k) clearance on 2016-04-07. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K160651.
When did BD FlowSmart Set, MiniMed Pro-Set receive FDA 510(k) clearance?
BD FlowSmart Set, MiniMed Pro-Set received FDA 510(k) clearance on 2016-04-07, under 510(k) number K160651.
Who is the listed applicant for BD FlowSmart Set, MiniMed Pro-Set?
The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD FlowSmart Set, MiniMed Pro-Set?
The FDA product code for BD FlowSmart Set, MiniMed Pro-Set is FPA.
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Becton, Dickinson and Company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:FPA)
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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