患者监护仪(CX10,CX12,CX15,UX10,UX12,UX15)
K号: K250179 · 2025-07-29
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器械摘要
常见问题
What is the Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15)?
Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15) is a medical device that received FDA 510(k) clearance on 2025-07-29. The listed applicant is Edan Instruments, Inc.. The 510(k) number is K250179.
When did Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15) receive FDA 510(k) clearance?
Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15) received FDA 510(k) clearance on 2025-07-29, under 510(k) number K250179.
Who is the listed applicant for Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15)?
FDA 510(k)记录中列出Edan Instruments, Inc.为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15)?
The FDA product code for Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15) is MHX.
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Edan Instruments, Inc.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:MHX)
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。
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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