FDA 510(k)

ACIST 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

K号: K252653 · 2026-05-13

决定日期2026-05-13

产品代码DXT

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 Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable 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 2026-05-13 under 510(k) number K252653. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable?

ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable is a medical device that received FDA 510(k) clearance on 2026-05-13. The listed applicant is Acist Medical Systems, Inc.. The 510(k) number is K252653.

When did ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable receive FDA 510(k) clearance?

ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable received FDA 510(k) clearance on 2026-05-13, under 510(k) number K252653.

Who is the listed applicant for ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable?

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 Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable?

The FDA product code for ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable is DXT.

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）K233904ACIST RXi 系统 (016616)；ACIST Navvus II 导管 (016675_)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：DXT）

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。

K252652用于电力注射器的配套一次性注射器（900103T）；用于电力注射器的配套一次性注射器（900103H）；用于电力注射器的配套一次性注射器（801800H）；用于电力注射器的配套一次性注射器（800099T）；用于电力注射器的配套一次性注射器（800099H）；用于电力注射器的配套一次性注射器（800096T）；用于电力注射器的配套一次性注射器（800096H）；一次性注射器配套Fortis Biosolutions Company Limited 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）Acist Medical Systems, Inc.K253048高压注射器；压力连接管；快速填充管；针头；转移管Shenzhen Maiwei Biotech Co., Ltd.K251788扩展管Zhuhai DR Medical Instruments Co., Ltd.K252891MEDRAD MRXperion MR 注射系统及 MR 注射系统注射器套件；MEDRAD ISI2 模块（ISI2）Bayer Medical Care, Inc.K244038高压软管Shandong Int Medical Instruments Co., Ltd.

官方来源

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