FLEX 微波消融系统及其附件
K号: K163118 · 2017-03-09
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器械摘要
常见问题
What is the FLEX Microwave Ablation System and Accessories?
FLEX Microwave Ablation System and Accessories is a medical device that received FDA 510(k) clearance on 2017-03-09. The listed applicant is Neuwave Medical, Inc.. The 510(k) number is K163118.
When did FLEX Microwave Ablation System and Accessories receive FDA 510(k) clearance?
FLEX Microwave Ablation System and Accessories received FDA 510(k) clearance on 2017-03-09, under 510(k) number K163118.
Who is the listed applicant for FLEX Microwave Ablation System and Accessories?
The FDA 510(k) record lists Neuwave Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEX Microwave Ablation System and Accessories?
The FDA product code for FLEX Microwave Ablation System and Accessories 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Neuwave Medical, 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。
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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