VPS节律设备,配备TipTracker技术
K号: K160925 · 2016-12-22
广告
器械摘要
常见问题
What is the VPS Rhythm Device with TipTracker Technology?
VPS Rhythm Device with TipTracker Technology is a medical device that received FDA 510(k) clearance on 2016-12-22. The listed applicant is Arrow International, Inc. (A Subsidiary of Teleflex, Inc.). The 510(k) number is K160925.
When did VPS Rhythm Device with TipTracker Technology receive FDA 510(k) clearance?
VPS Rhythm Device with TipTracker Technology received FDA 510(k) clearance on 2016-12-22, under 510(k) number K160925.
Who is the listed applicant for VPS Rhythm Device with TipTracker Technology?
The FDA 510(k) record lists Arrow International, Inc. (A Subsidiary of Teleflex, Inc.) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VPS Rhythm Device with TipTracker Technology?
The FDA product code for VPS Rhythm Device with TipTracker Technology is LJS.
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。
相关器械(代码:LJS)
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