FDA 510(k)美拉干系统
K号: K160141 · 2016-10-31
决定日期2016-10-31
产品代码NEY
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
miraDry System is the device name listed in this FDA 510(k) record. The listed applicant is Miramar Labs, Inc.. It received FDA 510(k) clearance on 2016-10-31 under 510(k) number K160141. 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 miraDry System?
miraDry System is a medical device that received FDA 510(k) clearance on 2016-10-31. The listed applicant is Miramar Labs, Inc.. The 510(k) number is K160141.
When did miraDry System receive FDA 510(k) clearance?
miraDry System received FDA 510(k) clearance on 2016-10-31, under 510(k) number K160141.
Who is the listed applicant for miraDry System?
The FDA 510(k) record lists Miramar Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for miraDry System?
The FDA product code for miraDry 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Miramar Labs, Inc.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。
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.K252632微波消融设备Nanjing Dewen 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.