FFR V2.5
K号: K170133 · 2017-05-26
广告
器械摘要
FFR V2.5 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Volcano. It received FDA 510(k) clearance on 2017-05-26 under 510(k) number K170133. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the FFR V2.5?
FFR V2.5 is a medical device that received FDA 510(k) clearance on 2017-05-26. The listed applicant is Philips Volcano. The 510(k) number is K170133.
When did FFR V2.5 receive FDA 510(k) clearance?
FFR V2.5 received FDA 510(k) clearance on 2017-05-26, under 510(k) number K170133.
Who is the listed applicant for FFR V2.5?
The FDA 510(k) record lists Philips Volcano as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FFR V2.5?
The FDA product code for FFR V2.5 is IYO.
列明Philips Volcano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：IYO）
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。
广告