PROTEUS PTA 气囊导管带栓塞捕获功能
K号: K172494 · 2017-12-15
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器械摘要
常见问题
What is the PROTEUS PTA Balloon Catheter with Embolic Capture Feature?
PROTEUS PTA Balloon Catheter with Embolic Capture Feature is a medical device that received FDA 510(k) clearance on 2017-12-15. The listed applicant is Angioslide, Ltd.. The 510(k) number is K172494.
When did PROTEUS PTA Balloon Catheter with Embolic Capture Feature receive FDA 510(k) clearance?
PROTEUS PTA Balloon Catheter with Embolic Capture Feature received FDA 510(k) clearance on 2017-12-15, under 510(k) number K172494.
Who is the listed applicant for PROTEUS PTA Balloon Catheter with Embolic Capture Feature?
The FDA 510(k) record lists Angioslide, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTEUS PTA Balloon Catheter with Embolic Capture Feature?
The FDA product code for PROTEUS PTA Balloon Catheter with Embolic Capture Feature is LIT.
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:LIT)
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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