FDA 510(k)

M3290B Philips IntelliVue 信息中心 iX

K号: K163584 · 2017-07-07

决定日期2017-07-07

产品代码MHX

咨询委员会CV 请注意，由于原文未提供具体内容，以下是一个示例翻译： --- 产品名称：[产品名称] 公司名称：[公司名称] FDA批准号：[FDA批准号] 510(k)申请号：[510(k)申请号] PMA申请号：[PMA申请号] 临床试验注册号：[NCT] PubMed ID：[PMID] 产品标识符：[标识符] 产品URL：[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。

决定实质等同

器械摘要

M3290B Philips IntelliVue Information Center iX is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2017-07-07 under 510(k) number K163584. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the M3290B Philips IntelliVue Information Center iX?

M3290B Philips IntelliVue Information Center iX is a medical device that received FDA 510(k) clearance on 2017-07-07. The listed applicant is Philips Medical Systems. The 510(k) number is K163584.

When did M3290B Philips IntelliVue Information Center iX receive FDA 510(k) clearance?

M3290B Philips IntelliVue Information Center iX received FDA 510(k) clearance on 2017-07-07, under 510(k) number K163584.

Who is the listed applicant for M3290B Philips IntelliVue Information Center iX?

The FDA 510(k) record lists Philips Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M3290B Philips IntelliVue Information Center iX?

The FDA product code for M3290B Philips IntelliVue Information Center iX is MHX.

列明Philips Medical Systems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。

K212704Philips EPIQ诊断超声系统，Philips Affiniti诊断超声系统 K211597EPIQ 系列诊断超声系统, Affiniti 系列诊断超声系统 K210560Page Writer TC20 心电图机，Page Writer TC30 心电图机，Page Writer TC50 心电图机，Page Writer TC70 心电图机 K191738PageWriter TC20 心电图机，PageWriter TC30 心电图机，PageWriter TC50 心电图机，PageWriter TC70 心电图机 K192875Philips Biosensor BX100 K183387M3290B Patient Information Center iX

查看所有 14 个设备 →

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。

K260656Carescape ONE；Carescape Dock F0；TruSignal ECG MM；TruSignal PRES MM；TruSignal TEMP MM；TruSignal SpO2 MM 1.8M；TruSignal SpO2 MM 3.0MGE Healthcare Finland Oy K260343Carescape Canvas 1000；Carescape Canvas智能显示屏GE Healthcare Finland Oy K260579Infinity® 急诊护理系统（IACS）- VG8.1Draeger Medical Systems, Inc.K251508遥测监测仪（iT30，iT50）Edan Instruments, Inc.K253277Monitor B105M；Monitor B125M；Monitor B155M；Monitor B105P；Monitor B125PGe Medical Systems Information Technologies, Inc.K254209Radius VSM和附件Masimo Corporation

官方来源

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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。