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FDA 510(k)

Abiomed 14Fr 低轮廓导引器套件

K号: K241708 · 2024-08-06

申请人Abiomed, Inc.
决定日期2024-08-06
产品代码DYB
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

Abiomed 14Fr Low Profile Introducer Kit is the device name listed in this FDA 510(k) record. The listed applicant is Abiomed, Inc.. It received FDA 510(k) clearance on 2024-08-06 under 510(k) number K241708. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Abiomed 14Fr Low Profile Introducer Kit?

Abiomed 14Fr Low Profile Introducer Kit is a medical device that received FDA 510(k) clearance on 2024-08-06. The listed applicant is Abiomed, Inc.. The 510(k) number is K241708.

When did Abiomed 14Fr Low Profile Introducer Kit receive FDA 510(k) clearance?

Abiomed 14Fr Low Profile Introducer Kit received FDA 510(k) clearance on 2024-08-06, under 510(k) number K241708.

Who is the listed applicant for Abiomed 14Fr Low Profile Introducer Kit?

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

What is the FDA product code for Abiomed 14Fr Low Profile Introducer Kit?

The FDA product code for Abiomed 14Fr Low Profile Introducer Kit is DYB.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Abiomed, Inc.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。

K25276614Fr 低轮廓引导器套装K221294preCARDIA 阻塞系统K223161OXY-1 系统K222113Abiomed 14Fr 低轮廓导引器套装K202330Impella XR 套管套装K200109OXY-1 系统

查看所有 9 个设备 →

相关器械（代码：DYB）

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。

K253526NAMIC 扩张器和套管Medline Industries, LPK261529微穿刺套件/微穿刺接入套件/微穿刺引导器套装/微引导器套件/微引导器套件（SIS05C）；微穿刺套件/微穿刺接入套件/微穿刺引导器套装/微引导器套件/微引导器套件（IS01）；引导器套件/微引导器套件/引导器套装/微引导器套装/微引导器鞘套装/引导器鞘套装（NIS04）Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line 可撕开引导器Health Line International CorporationK261492FieldFlex 可弯曲鞘CenterPoint Systems, LLCK260606Echo 大口径引导鞘Echo Medical, LLC

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。

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