LiverMultiScan v5 (LMSv5)
K号: K213960 · 2022-09-06
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器械摘要
LiverMultiScan v5 (LMSv5) is the device name listed in this FDA 510(k) record. The listed applicant is Perspectum. It received FDA 510(k) clearance on 2022-09-06 under 510(k) number K213960. 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 LiverMultiScan v5 (LMSv5)?
LiverMultiScan v5 (LMSv5) is a medical device that received FDA 510(k) clearance on 2022-09-06. The listed applicant is Perspectum. The 510(k) number is K213960.
When did LiverMultiScan v5 (LMSv5) receive FDA 510(k) clearance?
LiverMultiScan v5 (LMSv5) received FDA 510(k) clearance on 2022-09-06, under 510(k) number K213960.
Who is the listed applicant for LiverMultiScan v5 (LMSv5)?
The FDA 510(k) record lists Perspectum as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LiverMultiScan v5 (LMSv5)?
The FDA product code for LiverMultiScan v5 (LMSv5) is LNH.
相关临床试验
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列明Perspectum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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