FDA 510(k)

多链X2心电图适配器和直接连接导线系统

K号: K163316 · 2017-06-22

决定日期2017-06-22

产品代码DSA

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

Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System is the device name listed in this FDA 510(k) record. The listed applicant is Carefusion 303, Inc.. It received FDA 510(k) clearance on 2017-06-22 under 510(k) number K163316. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System?

Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System is a medical device that received FDA 510(k) clearance on 2017-06-22. The listed applicant is Carefusion 303, Inc.. The 510(k) number is K163316.

When did Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System receive FDA 510(k) clearance?

Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System received FDA 510(k) clearance on 2017-06-22, under 510(k) number K163316.

Who is the listed applicant for Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System?

The FDA 510(k) record lists Carefusion 303, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System?

The FDA product code for Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System is DSA.

列明Carefusion 303, 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。

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相关器械（代码：DSA）

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

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