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FDA 510(k)

ACIST RXi 系统 (016616)；ACIST Navvus II 导管 (016675_)

K号: K233904 · 2024-07-17

申请人Acist Medical Systems, Inc.
决定日期2024-07-17
产品代码DXO
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

ACIST RXi System (016616); ACIST Navvus II Catheter (016675_ is the device name listed in this FDA 510(k) record. The listed applicant is Acist Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-07-17 under 510(k) number K233904. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ACIST RXi System (016616); ACIST Navvus II Catheter (016675_?

ACIST RXi System (016616); ACIST Navvus II Catheter (016675_ is a medical device that received FDA 510(k) clearance on 2024-07-17. The listed applicant is Acist Medical Systems, Inc.. The 510(k) number is K233904.

When did ACIST RXi System (016616); ACIST Navvus II Catheter (016675_ receive FDA 510(k) clearance?

ACIST RXi System (016616); ACIST Navvus II Catheter (016675_ received FDA 510(k) clearance on 2024-07-17, under 510(k) number K233904.

Who is the listed applicant for ACIST RXi System (016616); ACIST Navvus II Catheter (016675_?

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

What is the FDA product code for ACIST RXi System (016616); ACIST Navvus II Catheter (016675_?

The FDA product code for ACIST RXi System (016616); ACIST Navvus II Catheter (016675_ is DXO.

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Acist Medical Systems, 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。

K262115VueJect® 超声增强剂输送系统K252638VeraPro S100 多功能注射器（018808）；VeraPro S100 LV1 低粘度一次性注射器（018811）；VeraPro AMT 自动分路器和传感器（018814）；VeraPro AngioTouch FLX165 手控器套件（018806）；VeraPro AngioTouch HiFi165 手控器套件（018804）K252653ACIST Pro 诊断系统 (019304)；处理单元床架；AngioTouch 模块；ACIST Pro 手推车；单探头电缆；三探头电缆K203004ACIST CVi1 对比剂输送系统，ACIST CVi 对比剂输送系统K193183ACIST HDi 系统，ACIST Kodama 内窥镜超声导管K190473ACIST RXi 系统和 Navvus II 导管

查看所有 12 个设备 →

相关器械（代码：DXO）

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。

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K222216TruWave 一次性压力传感器Edwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, Inc.K193279Comet II 压力导丝Boston Scientific Corporation

官方来源

在 FDA 数据库中查看 →

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