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FDA 510(k)

维纳欧系统(00MEDRF4000TCUS 05CR45iT 06Pedal1St)

K号: K253918 · 2026-06-02

决定日期2026-06-02
产品代码GEI
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) is the device name listed in this FDA 510(k) record. The listed applicant is F Care Systems USA, LLC. It received FDA 510(k) clearance on 2026-06-02 under 510(k) number K253918. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)?

Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) is a medical device that received FDA 510(k) clearance on 2026-06-02. The listed applicant is F Care Systems USA, LLC. The 510(k) number is K253918.

When did Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) receive FDA 510(k) clearance?

Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) received FDA 510(k) clearance on 2026-06-02, under 510(k) number K253918.

Who is the listed applicant for Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)?

The FDA 510(k) record lists F Care Systems USA, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)?

The FDA product code for Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) is GEI.

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。

列明F Care Systems USA, LLC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。

相关器械(代码:GEI)

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。

官方来源

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