Polux、Minerva 和 Atropos PTA 扩张球囊导管
K号: K160256 · 2016-07-29
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器械摘要
常见问题
What is the Polux , Minerva and Atropos PTA Balloon Dilatation Catheter?
Polux , Minerva and Atropos PTA Balloon Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2016-07-29. The listed applicant is Brosmed Medical Co., Ltd.. The 510(k) number is K160256.
When did Polux , Minerva and Atropos PTA Balloon Dilatation Catheter receive FDA 510(k) clearance?
Polux , Minerva and Atropos PTA Balloon Dilatation Catheter received FDA 510(k) clearance on 2016-07-29, under 510(k) number K160256.
Who is the listed applicant for Polux , Minerva and Atropos PTA Balloon Dilatation Catheter?
The FDA 510(k) record lists Brosmed Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Polux , Minerva and Atropos PTA Balloon Dilatation Catheter?
The FDA product code for Polux , Minerva and Atropos PTA Balloon Dilatation Catheter 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。
列明Brosmed Medical Co., Ltd.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: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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