Finapres Nova 非侵入性血流动力学监测仪
K号: K160967 · 2017-04-18
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器械摘要
常见问题
What is the Finapres Nova Noninvasive Hemodynamic Monitor?
Finapres Nova Noninvasive Hemodynamic Monitor is a medical device that received FDA 510(k) clearance on 2017-04-18. The listed applicant is Finapres Medical Systems B.V.. The 510(k) number is K160967.
When did Finapres Nova Noninvasive Hemodynamic Monitor receive FDA 510(k) clearance?
Finapres Nova Noninvasive Hemodynamic Monitor received FDA 510(k) clearance on 2017-04-18, under 510(k) number K160967.
Who is the listed applicant for Finapres Nova Noninvasive Hemodynamic Monitor?
The FDA 510(k) record lists Finapres Medical Systems B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Finapres Nova Noninvasive Hemodynamic Monitor?
The FDA product code for Finapres Nova Noninvasive Hemodynamic Monitor is DXN.
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Finapres Medical Systems B.V.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:DXN)
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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