FDA 510(k)

维纳斯608深静脉血栓（DVT）预防系统

K号: K241096 · 2025-01-15

申请人Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

决定日期2025-01-15

产品代码JOW

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

Venera 608 Deep Vein Thrombosis (DVT) Prevention System is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. It received FDA 510(k) clearance on 2025-01-15 under 510(k) number K241096. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

Venera 608 Deep Vein Thrombosis (DVT) Prevention System is a medical device that received FDA 510(k) clearance on 2025-01-15. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K241096.

When did Venera 608 Deep Vein Thrombosis (DVT) Prevention System receive FDA 510(k) clearance?

Venera 608 Deep Vein Thrombosis (DVT) Prevention System received FDA 510(k) clearance on 2025-01-15, under 510(k) number K241096.

Who is the listed applicant for Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

The FDA 510(k) record lists Suzhou Minhua Medical Apparatus Supplies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

The FDA product code for Venera 608 Deep Vein Thrombosis (DVT) Prevention System is JOW.

列明Suzhou Minhua Medical Apparatus Supplies Co., Ltd.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。

K233276可重复使用血压袖带 K180389维纳斯508深静脉血栓（DVT）预防系统 K171889可重复使用血压袖带

官方来源

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