Clip Flow
K号: K153493 · 2016-07-29
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器械摘要
Clip Flow is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2016-07-29 under 510(k) number K153493. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Clip Flow?
Clip Flow is a medical device that received FDA 510(k) clearance on 2016-07-29. The listed applicant is Voco GmbH. The 510(k) number is K153493.
When did Clip Flow receive FDA 510(k) clearance?
Clip Flow received FDA 510(k) clearance on 2016-07-29, under 510(k) number K153493.
Who is the listed applicant for Clip Flow?
The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Clip Flow?
The FDA product code for Clip Flow is EBF.
列明Voco GmbH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：EBF）
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。
K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, Inc.
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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