AnastoClip GC闭合系统
K号: K173323 · 2018-03-08
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决定日期2018-03-08
产品代码FZP
咨询委员会SU
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决定实质等同
器械摘要
AnastoClip GC Closure System is the device name listed in this FDA 510(k) record. The listed applicant is LeMaitre Vascular, Inc.. It received FDA 510(k) clearance on 2018-03-08 under 510(k) number K173323. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AnastoClip GC Closure System?
AnastoClip GC Closure System is a medical device that received FDA 510(k) clearance on 2018-03-08. The listed applicant is LeMaitre Vascular, Inc.. The 510(k) number is K173323.
When did AnastoClip GC Closure System receive FDA 510(k) clearance?
AnastoClip GC Closure System received FDA 510(k) clearance on 2018-03-08, under 510(k) number K173323.
Who is the listed applicant for AnastoClip GC Closure System?
The FDA 510(k) record lists LeMaitre Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AnastoClip GC Closure System?
The FDA product code for AnastoClip GC Closure System is FZP.
相关临床试验
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列明LeMaitre Vascular, 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：FZP）
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。
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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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