G-scan Brio
K号: K180592 · 2018-03-30
广告
器械摘要
G-scan Brio is the device name listed in this FDA 510(k) record. The listed applicant is Esaote, S.p.A.. It received FDA 510(k) clearance on 2018-03-30 under 510(k) number K180592. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the G-scan Brio?
G-scan Brio is a medical device that received FDA 510(k) clearance on 2018-03-30. The listed applicant is Esaote, S.p.A.. The 510(k) number is K180592.
When did G-scan Brio receive FDA 510(k) clearance?
G-scan Brio received FDA 510(k) clearance on 2018-03-30, under 510(k) number K180592.
Who is the listed applicant for G-scan Brio?
FDA 510(k)记录中列出Esaote, S.p.A.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 G-scan Brio?
The FDA product code for G-scan Brio is LNH.
列明Esaote, S.p.A.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：LNH）
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。
K261283APERTO 明亮 MRI 系统Fujifilm CorporationK261758拥抱愿景新生儿MRI系统Aspect Imaging, Ltd.K260758MAGNETOM Free.Max; MAGNETOM Free.StarSiemens Shenzhen Magnetic Resonance , Ltd.K262622Swoop® 便携式MR成像® 系统Hyperfine, Inc.K254250MagicScan-1.5，GreenMR宁静1.5TXingaoyi Medical Equipment Co.,LtdK253808AIR Recon DLGE Medical Systems
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