维纳欧系统(00MEDRF4000TCUS 05CR45iT 06Pedal1St)
K号: K253918 · 2026-06-02
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器械摘要
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
在 FDA 数据库中查看 →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。
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