Geneva
K号: K201272 · 2020-07-16
广告
器械摘要
Geneva is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron B.V.. It received FDA 510(k) clearance on 2020-07-16 under 510(k) number K201272. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Geneva?
Geneva is a medical device that received FDA 510(k) clearance on 2020-07-16. The listed applicant is Nucletron B.V.. The 510(k) number is K201272.
When did Geneva receive FDA 510(k) clearance?
Geneva received FDA 510(k) clearance on 2020-07-16, under 510(k) number K201272.
Who is the listed applicant for Geneva?
FDA 510(k)记录中列出Nucletron B.V.为申请人。这本身并不能确立该设备的制造商。
What is the FDA product code for Geneva?
The FDA product code for Geneva is JAQ.
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Nucletron 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：JAQ）
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。
广告