swiftPro™ 系统
K号: K240518 · 2024-04-23
广告
器械摘要
swiftPro™ System is the device name listed in this FDA 510(k) record. The listed applicant is Emblation Limited. It received FDA 510(k) clearance on 2024-04-23 under 510(k) number K240518. The device is classified under product code NEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the swiftPro™ System?
swiftPro™ System is a medical device that received FDA 510(k) clearance on 2024-04-23. The listed applicant is Emblation Limited. The 510(k) number is K240518.
When did swiftPro™ System receive FDA 510(k) clearance?
swiftPro™ System received FDA 510(k) clearance on 2024-04-23, under 510(k) number K240518.
Who is the listed applicant for swiftPro™ System?
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?
The FDA product code for swiftPro™ System 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。
K252632微波消融设备Nanjing Dewen Medical Technology Co., Ltd.K253771一次性微波消融天线（DW-XR-II1, DW-XR-II3, DW-XR-II4, DW-XR-II14, DW-XR-II5, DW-XR-II6, DW-XR-II7, DW-XR-II8, DW-XR-II9, DW-XR-II10, DW-XR-II18, DW-XR-II19, DW-XR-II20, DW-XR-II21, DW-DG-II6, DW-DG-II7, DW-DG-II9, DW-DG-II10, DW-DG-II13）Nanjing Devin Medical Technology Co., Ltd.K250718swiftPro系统（SWF-SPS）；Swift系统（SWF-SYS）Emblation LimitedK241827微波消融发生器（KY-2000A, KY-2100A）Canyon Medical, Inc.K241825Microwave Ablation AntennasCanyon Medical, Inc.K240480IntelliBlate 微波消融系统控制台 (IB-CON)；IntelliBlate 微波消融系统移动车 (IB-CART)；IntelliBlate Ximitry 探头组件，13G x 15cm (IB-XPA-1315)；IntelliBlate Ximitry 探头组件，13G x 20cm (IB-XPA-1320)；IntelliBlate Ximitry 探头组件，13G x 27cm (IB-XPA-1327)Varian Medical Systems, Inc.
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。
广告