FDA 510(k)

LiDCOunity v2 血流动力学监视器

K号: K163334 · 2017-06-05

决定日期2017-06-05

产品代码DXG

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

LiDCOunity v2 Hemodynamic Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Lidco, Ltd.. It received FDA 510(k) clearance on 2017-06-05 under 510(k) number K163334. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LiDCOunity v2 Hemodynamic Monitor?

LiDCOunity v2 Hemodynamic Monitor is a medical device that received FDA 510(k) clearance on 2017-06-05. The listed applicant is Lidco, Ltd.. The 510(k) number is K163334.

When did LiDCOunity v2 Hemodynamic Monitor receive FDA 510(k) clearance?

LiDCOunity v2 Hemodynamic Monitor received FDA 510(k) clearance on 2017-06-05, under 510(k) number K163334.

Who is the listed applicant for LiDCOunity v2 Hemodynamic Monitor?

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

What is the FDA product code for LiDCOunity v2 Hemodynamic Monitor?

The FDA product code for LiDCOunity v2 Hemodynamic Monitor is DXG.

列明Lidco, Ltd.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。

K152935LiDCOunity 监视器

官方来源

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