免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

YP-710T系列血压计袖带;YP-840T系列一次性袖带

K号: K260747 · 2026-05-06

决定日期2026-05-06
产品代码DXQ
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

YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Corporation. It received FDA 510(k) clearance on 2026-05-06 under 510(k) number K260747. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff?

YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff is a medical device that received FDA 510(k) clearance on 2026-05-06. The listed applicant is Nihon Kohden Corporation. The 510(k) number is K260747.

When did YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff receive FDA 510(k) clearance?

YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff received FDA 510(k) clearance on 2026-05-06, under 510(k) number K260747.

Who is the listed applicant for YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff?

FDA 510(k)记录中列出Nihon Kohden Corporation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 YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff?

The FDA product code for YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff is DXQ.

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Nihon Kohden Corporation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。

查看所有 19 个设备 →

相关器械(代码:DXQ)

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

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。

↑