FDA 510(k)

ZOLL心律管理系统

K号: K190939 · 2019-12-19

决定日期2019-12-19

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

ZOLL Arrhythmia Management Sysyem is the device name listed in this FDA 510(k) record. The listed applicant is Zoll Manufacturing Corporation. It received FDA 510(k) clearance on 2019-12-19 under 510(k) number K190939. 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 ZOLL Arrhythmia Management Sysyem?

ZOLL Arrhythmia Management Sysyem is a medical device that received FDA 510(k) clearance on 2019-12-19. The listed applicant is Zoll Manufacturing Corporation. The 510(k) number is K190939.

When did ZOLL Arrhythmia Management Sysyem receive FDA 510(k) clearance?

ZOLL Arrhythmia Management Sysyem received FDA 510(k) clearance on 2019-12-19, under 510(k) number K190939.

Who is the listed applicant for ZOLL Arrhythmia Management Sysyem?

The FDA 510(k) record lists Zoll Manufacturing Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZOLL Arrhythmia Management Sysyem?

The FDA product code for ZOLL Arrhythmia Management Sysyem is MHX.

列明Zoll Manufacturing Corporation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。

K182093ZOLL心电图分析软件 K172510µCor 心力衰竭和心律失常管理系统

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

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。