SIGNA™ Sprint Select
K号: K253779 · 2026-02-05
广告
器械摘要
SIGNA™ Sprint Select is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems, LLC. It received FDA 510(k) clearance on 2026-02-05 under 510(k) number K253779. 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 SIGNA™ Sprint Select?
SIGNA™ Sprint Select is a medical device that received FDA 510(k) clearance on 2026-02-05. The listed applicant is Ge Medical Systems, LLC. The 510(k) number is K253779.
When did SIGNA™ Sprint Select receive FDA 510(k) clearance?
SIGNA™ Sprint Select received FDA 510(k) clearance on 2026-02-05, under 510(k) number K253779.
Who is the listed applicant for SIGNA™ Sprint Select?
The FDA 510(k) record lists Ge Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIGNA™ Sprint Select?
The FDA product code for SIGNA™ Sprint Select 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Ge Medical Systems, LLC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