1.5T 24E 后置阵列
K号: K223203 · 2023-03-02
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器械摘要
1.5T 24E Posterior Array is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen RF Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-03-02 under 510(k) number K223203. 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 1.5T 24E Posterior Array?
1.5T 24E Posterior Array is a medical device that received FDA 510(k) clearance on 2023-03-02. The listed applicant is Shenzhen RF Tech Co., Ltd.. The 510(k) number is K223203.
When did 1.5T 24E Posterior Array receive FDA 510(k) clearance?
1.5T 24E Posterior Array received FDA 510(k) clearance on 2023-03-02, under 510(k) number K223203.
Who is the listed applicant for 1.5T 24E Posterior Array?
The FDA 510(k) record lists Shenzhen RF Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1.5T 24E Posterior Array?
The FDA product code for 1.5T 24E Posterior Array is LNH.
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Shenzhen RF Tech Co., Ltd.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。
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