FDA 510(k)

全自动（NIBP）血压计，型号HL858DM

K号: K211127 · 2021-09-08

决定日期2021-09-08

产品代码DXN

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

Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM is the device name listed in this FDA 510(k) record. The listed applicant is Health & Life Co., Ltd.. It received FDA 510(k) clearance on 2021-09-08 under 510(k) number K211127. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM?

Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM is a medical device that received FDA 510(k) clearance on 2021-09-08. The listed applicant is Health & Life Co., Ltd.. The 510(k) number is K211127.

When did Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM receive FDA 510(k) clearance?

Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM received FDA 510(k) clearance on 2021-09-08, under 510(k) number K211127.

Who is the listed applicant for Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM?

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

What is the FDA product code for Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM?

The FDA product code for Full Automatic (NIBP) Blood Pressure Monitor, Model HL858DM is DXN.

列明Health & Life Co., 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。

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相关器械（代码：DXN）

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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