Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector
K号: K213089 · 2021-11-10
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器械摘要
常见问题
What is the Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector?
Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector is a medical device that received FDA 510(k) clearance on 2021-11-10. The listed applicant is Ivenix, Inc.. The 510(k) number is K213089.
When did Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector receive FDA 510(k) clearance?
Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector received FDA 510(k) clearance on 2021-11-10, under 510(k) number K213089.
Who is the listed applicant for Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector?
The FDA 510(k) record lists Ivenix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector?
The FDA product code for Ivenix Infusion System, LVP Epidural Administraion Set NRFit Connector is FPA.
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列明Ivenix, Inc.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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