CT Expres 3D对比剂输送系统,瓶式刺针型B,Day Set III HP,患者套装
K号: K151048 · 2016-01-22
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器械摘要
常见问题
What is the CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set?
CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set is a medical device that received FDA 510(k) clearance on 2016-01-22. The listed applicant is Bracco Injeneering. The 510(k) number is K151048.
When did CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set receive FDA 510(k) clearance?
CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set received FDA 510(k) clearance on 2016-01-22, under 510(k) number K151048.
Who is the listed applicant for CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set?
The FDA 510(k) record lists Bracco Injeneering as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set?
The FDA product code for CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set is IZQ.
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。
相关器械(代码:IZQ)
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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