PathBuilder 经房间隔引导导丝
K号: K212626 · 2022-03-23
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器械摘要
常见问题
What is the PathBuilder Transseptal Guiding Introducer?
PathBuilder Transseptal Guiding Introducer is a medical device that received FDA 510(k) clearance on 2022-03-23. The listed applicant is Shanghai Microport EP Medtech Co., Ltd.. The 510(k) number is K212626.
When did PathBuilder Transseptal Guiding Introducer receive FDA 510(k) clearance?
PathBuilder Transseptal Guiding Introducer received FDA 510(k) clearance on 2022-03-23, under 510(k) number K212626.
Who is the listed applicant for PathBuilder Transseptal Guiding Introducer?
The FDA 510(k) record lists Shanghai Microport EP Medtech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PathBuilder Transseptal Guiding Introducer?
The FDA product code for PathBuilder Transseptal Guiding Introducer is DYB.
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Shanghai Microport EP Medtech 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:DYB)
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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