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FDA 510(k)

Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl

K号: K170873 · 2017-10-02

申请人Swissmeditec GmbH
决定日期2017-10-02
产品代码EBF
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决定实质等同

器械摘要

Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl is the device name listed in this FDA 510(k) record. The listed applicant is Swissmeditec GmbH. It received FDA 510(k) clearance on 2017-10-02 under 510(k) number K170873. 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 Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl?

Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl is a medical device that received FDA 510(k) clearance on 2017-10-02. The listed applicant is Swissmeditec GmbH. The 510(k) number is K170873.

When did Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl receive FDA 510(k) clearance?

Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl received FDA 510(k) clearance on 2017-10-02, under 510(k) number K170873.

Who is the listed applicant for Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl?

The FDA 510(k) record lists Swissmeditec GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl?

The FDA product code for Medi Galaxy Flow, Medi Classic, Medi Pearl, Medi Jupiter, Medi Opaque Posterior, Medi White Pearl is EBF.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

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 双核Spident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695流动修复材料（KP-Flow LF，KP-Flow MF，KP-Flow HF）Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228超越大体积填充流动复合树脂Ultradent Products, Inc.K261246SRGC-06GC America, Inc.

官方来源

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