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FDA 510(k)

优威尔® 电子血压计(YE630CR)

K号: K252779 · 2026-03-05

决定日期2026-03-05
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

YUWELL® Electronic Blood Pressure Monitor (YE630CR) is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. It received FDA 510(k) clearance on 2026-03-05 under 510(k) number K252779. 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 YUWELL® Electronic Blood Pressure Monitor (YE630CR)?

YUWELL® Electronic Blood Pressure Monitor (YE630CR) is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. The 510(k) number is K252779.

When did YUWELL® Electronic Blood Pressure Monitor (YE630CR) receive FDA 510(k) clearance?

YUWELL® Electronic Blood Pressure Monitor (YE630CR) received FDA 510(k) clearance on 2026-03-05, under 510(k) number K252779.

Who is the listed applicant for YUWELL® Electronic Blood Pressure Monitor (YE630CR)?

FDA 510(k)记录将江苏宇悦医疗设备供应有限公司列为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for YUWELL® Electronic Blood Pressure Monitor (YE630CR)?

The FDA product code for YUWELL® Electronic Blood Pressure Monitor (YE630CR) is DXN.

相关临床试验

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。

列明Jiangsu Yuyue Medical Equipment & Supply 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。

官方来源

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