MAGNETOM Flow.Ace; MAGNETOM Flow.Plus
K号: K250436 · 2025-06-16
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器械摘要
MAGNETOM Flow.Ace; MAGNETOM Flow.Plus is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Shenzhen Magnetic Resonance , Ltd.. It received FDA 510(k) clearance on 2025-06-16 under 510(k) number K250436. 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 MAGNETOM Flow.Ace; MAGNETOM Flow.Plus?
MAGNETOM Flow.Ace; MAGNETOM Flow.Plus is a medical device that received FDA 510(k) clearance on 2025-06-16. The listed applicant is Siemens Shenzhen Magnetic Resonance , Ltd.. The 510(k) number is K250436.
When did MAGNETOM Flow.Ace; MAGNETOM Flow.Plus receive FDA 510(k) clearance?
MAGNETOM Flow.Ace; MAGNETOM Flow.Plus received FDA 510(k) clearance on 2025-06-16, under 510(k) number K250436.
Who is the listed applicant for MAGNETOM Flow.Ace; MAGNETOM Flow.Plus?
FDA 510(k)记录将深圳西门子磁共振有限公司列为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for MAGNETOM Flow.Ace; MAGNETOM Flow.Plus?
The FDA product code for MAGNETOM Flow.Ace; MAGNETOM Flow.Plus 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Siemens Shenzhen Magnetic Resonance , 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。
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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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