Coldplay Cryoballoon 激光消融系统;焦点消融系统,全面消融系统;Swipe 消融系统
K号: K152329 · 2016-04-13
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器械摘要
常见问题
What is the Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System?
Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System is a medical device that received FDA 510(k) clearance on 2016-04-13. The listed applicant is C2 Therapeutics, Inc.. The 510(k) number is K152329.
When did Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System receive FDA 510(k) clearance?
Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System received FDA 510(k) clearance on 2016-04-13, under 510(k) number K152329.
Who is the listed applicant for Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System?
The FDA 510(k) record lists C2 Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System?
The FDA product code for Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System is GEH.
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C2 Therapeutics, 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:GEH)
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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