Paladin颈动脉后扩张球囊系统,带集成栓塞保护
K号: K221339 · 2022-06-09
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器械摘要
常见问题
What is the Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection?
Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection is a medical device that received FDA 510(k) clearance on 2022-06-09. The listed applicant is Contego Medical, Inc.. The 510(k) number is K221339.
When did Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection receive FDA 510(k) clearance?
Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection received FDA 510(k) clearance on 2022-06-09, under 510(k) number K221339.
Who is the listed applicant for Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection?
The FDA 510(k) record lists Contego Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection?
The FDA product code for Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection 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Contego Medical, 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: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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