FDA 510(k)

TriSalus TriNav® LV 静脉输液系统

K号: K230957 · 2023-05-02

决定日期2023-05-02

产品代码KRA

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

TriSalus TriNav® LV Infusion System is the device name listed in this FDA 510(k) record. The listed applicant is Trisalus Life Sciences. It received FDA 510(k) clearance on 2023-05-02 under 510(k) number K230957. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TriSalus TriNav® LV Infusion System?

TriSalus TriNav® LV Infusion System is a medical device that received FDA 510(k) clearance on 2023-05-02. The listed applicant is Trisalus Life Sciences. The 510(k) number is K230957.

When did TriSalus TriNav® LV Infusion System receive FDA 510(k) clearance?

TriSalus TriNav® LV Infusion System received FDA 510(k) clearance on 2023-05-02, under 510(k) number K230957.

Who is the listed applicant for TriSalus TriNav® LV Infusion System?

FDA 510(k)记录显示Trisalus Life Sciences为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for TriSalus TriNav® LV Infusion System?

The FDA product code for TriSalus TriNav® LV Infusion System is KRA.

列明Trisalus Life Sciences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。

K253509TriSalus TriNav Advance 注射系统 K233858TriSalus TriGuide™ 导丝引导导管 K193107TriSalus输液系统

官方来源

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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。