成人骨内输液装置
K号: K182770 · 2019-04-09
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器械摘要
常见问题
What is the Adult Intraosseous Infusion Device?
Adult Intraosseous Infusion Device is a medical device that received FDA 510(k) clearance on 2019-04-09. The listed applicant is Einstein Works, LLC. The 510(k) number is K182770.
When did Adult Intraosseous Infusion Device receive FDA 510(k) clearance?
Adult Intraosseous Infusion Device received FDA 510(k) clearance on 2019-04-09, under 510(k) number K182770.
Who is the listed applicant for Adult Intraosseous Infusion Device?
The FDA 510(k) record lists Einstein Works, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Adult Intraosseous Infusion Device?
The FDA product code for Adult Intraosseous Infusion Device 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Einstein Works, 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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