swiftPro系统(SWF-SPS);Swift系统(SWF-SYS)
K号: K250718 · 2025-08-08
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器械摘要
常见问题
What is the swiftPro System (SWF-SPS); Swift System (SWF-SYS)?
swiftPro System (SWF-SPS); Swift System (SWF-SYS) is a medical device that received FDA 510(k) clearance on 2025-08-08. The listed applicant is Emblation Limited. The 510(k) number is K250718.
When did swiftPro System (SWF-SPS); Swift System (SWF-SYS) receive FDA 510(k) clearance?
swiftPro System (SWF-SPS); Swift System (SWF-SYS) received FDA 510(k) clearance on 2025-08-08, under 510(k) number K250718.
Who is the listed applicant for swiftPro System (SWF-SPS); Swift System (SWF-SYS)?
The FDA 510(k) record lists Emblation Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for swiftPro System (SWF-SPS); Swift System (SWF-SYS)?
The FDA product code for swiftPro System (SWF-SPS); Swift System (SWF-SYS) is NEY.
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Emblation Limited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:NEY)
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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