Bard Power-Injectable Implantable Ports (PowerPorts®)
K号: K181446 · 2019-07-08
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器械摘要
常见问题
What is the Bard Power-Injectable Implantable Ports (PowerPorts®)?
Bard Power-Injectable Implantable Ports (PowerPorts®) is a medical device that received FDA 510(k) clearance on 2019-07-08. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K181446.
When did Bard Power-Injectable Implantable Ports (PowerPorts®) receive FDA 510(k) clearance?
Bard Power-Injectable Implantable Ports (PowerPorts®) received FDA 510(k) clearance on 2019-07-08, under 510(k) number K181446.
Who is the listed applicant for Bard Power-Injectable Implantable Ports (PowerPorts®)?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bard Power-Injectable Implantable Ports (PowerPorts®)?
The FDA product code for Bard Power-Injectable Implantable Ports (PowerPorts®) is LJT.
相关临床试验
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列明C.R. Bard, 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:LJT)
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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