FDA 510(k)

Carpentier-Edwards Physio Annuloplasty Ring (4450)

K号: K251688 · 2025-09-17

决定日期2025-09-17

产品代码KRH

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

Carpentier-Edwards Physio Annuloplasty Ring (4450) is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Lifesciences, LLC. It received FDA 510(k) clearance on 2025-09-17 under 510(k) number K251688. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Carpentier-Edwards Physio Annuloplasty Ring (4450)?

Carpentier-Edwards Physio Annuloplasty Ring (4450) is a medical device that received FDA 510(k) clearance on 2025-09-17. The listed applicant is Edwards Lifesciences, LLC. The 510(k) number is K251688.

When did Carpentier-Edwards Physio Annuloplasty Ring (4450) receive FDA 510(k) clearance?

Carpentier-Edwards Physio Annuloplasty Ring (4450) received FDA 510(k) clearance on 2025-09-17, under 510(k) number K251688.

Who is the listed applicant for Carpentier-Edwards Physio Annuloplasty Ring (4450)?

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

What is the FDA product code for Carpentier-Edwards Physio Annuloplasty Ring (4450)?

The FDA product code for Carpentier-Edwards Physio Annuloplasty Ring (4450) is KRH.

列明Edwards Lifesciences, LLC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。

K251326呼吸频率算法 K253186HemoSphere Nano监测仪（HSNANO1）K251982Edwards MC3 三尖瓣成形环（4900）K242518高血压预测指数（HePI）算法 K242909FloTrac 传感器；FloTrac Jr 传感器；Acumen IQ 传感器；VolumeView 传感器 K240078Fogarty 穿透管腔取栓导管

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