Venclose 射频系统(digiRF 发生器,EVSRF 电极导管)
K号: K160754 · 2016-09-09
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器械摘要
常见问题
What is the Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter)?
Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter) is a medical device that received FDA 510(k) clearance on 2016-09-09. The listed applicant is Venclose, Inc.. The 510(k) number is K160754.
When did Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter) receive FDA 510(k) clearance?
Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter) received FDA 510(k) clearance on 2016-09-09, under 510(k) number K160754.
Who is the listed applicant for Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter)?
The FDA 510(k) record lists Venclose, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter)?
The FDA product code for Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter) is GEI.
相关临床试验
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列明Venclose, 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: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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