FDA 510(k)

RX-1 Rhythm Express 远程心脏监护系统

K号: K200833 · 2020-09-02

决定日期2020-09-02

产品代码MLO

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

RX-1 Rhythm Express Remote Cardiac Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is VivaQuant, Inc.. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K200833. The device is classified under product code MLO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the RX-1 Rhythm Express Remote Cardiac Monitoring System?

RX-1 Rhythm Express Remote Cardiac Monitoring System is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is VivaQuant, Inc.. The 510(k) number is K200833.

When did RX-1 Rhythm Express Remote Cardiac Monitoring System receive FDA 510(k) clearance?

RX-1 Rhythm Express Remote Cardiac Monitoring System received FDA 510(k) clearance on 2020-09-02, under 510(k) number K200833.

Who is the listed applicant for RX-1 Rhythm Express Remote Cardiac Monitoring System?

The FDA 510(k) record lists VivaQuant, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RX-1 Rhythm Express Remote Cardiac Monitoring System?

The FDA product code for RX-1 Rhythm Express Remote Cardiac Monitoring System is MLO.

列明VivaQuant, 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。

K241179Rhythm Express 远程心脏监护系统 (RX-1 mini)K183704RX-1 Rhythm Express 远程心脏监护系统

官方来源

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