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:
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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]
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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。
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