Vas-Q-Clip
K号: K151943 · 2016-03-25
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决定日期2016-03-25
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
Vas-Q-Clip is the device name listed in this FDA 510(k) record. The listed applicant is Nanova Biomaterials, Inc.. It received FDA 510(k) clearance on 2016-03-25 under 510(k) number K151943. 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 Vas-Q-Clip?
Vas-Q-Clip is a medical device that received FDA 510(k) clearance on 2016-03-25. The listed applicant is Nanova Biomaterials, Inc.. The 510(k) number is K151943.
When did Vas-Q-Clip receive FDA 510(k) clearance?
Vas-Q-Clip received FDA 510(k) clearance on 2016-03-25, under 510(k) number K151943.
Who is the listed applicant for Vas-Q-Clip?
The FDA 510(k) record lists Nanova Biomaterials, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vas-Q-Clip?
The FDA product code for Vas-Q-Clip is FZP.
列明Nanova Biomaterials, 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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