EKOS 超声 EVD 设备,EVD 控制单元
K号: K172035 · 2018-03-24
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器械摘要
常见问题
What is the EKOS ultrasound EVD Device, EVD Control Unit?
EKOS ultrasound EVD Device, EVD Control Unit is a medical device that received FDA 510(k) clearance on 2018-03-24. The listed applicant is Btg International, Inc.. The 510(k) number is K172035.
When did EKOS ultrasound EVD Device, EVD Control Unit receive FDA 510(k) clearance?
EKOS ultrasound EVD Device, EVD Control Unit received FDA 510(k) clearance on 2018-03-24, under 510(k) number K172035.
Who is the listed applicant for EKOS ultrasound EVD Device, EVD Control Unit?
The FDA 510(k) record lists Btg International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EKOS ultrasound EVD Device, EVD Control Unit?
The FDA product code for EKOS ultrasound EVD Device, EVD Control Unit is JXG.
相关临床试验
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列明Btg International, 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:JXG)
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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