Jensen 遮光液体
K号: K183408 · 2019-03-20
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决定日期2019-03-20
产品代码EIH
咨询委员会DE
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决定实质等同
器械摘要
Jensen Shade Effect Liquids is the device name listed in this FDA 510(k) record. The listed applicant is Jensen Industries, Inc.. It received FDA 510(k) clearance on 2019-03-20 under 510(k) number K183408. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Jensen Shade Effect Liquids?
Jensen Shade Effect Liquids is a medical device that received FDA 510(k) clearance on 2019-03-20. The listed applicant is Jensen Industries, Inc.. The 510(k) number is K183408.
When did Jensen Shade Effect Liquids receive FDA 510(k) clearance?
Jensen Shade Effect Liquids received FDA 510(k) clearance on 2019-03-20, under 510(k) number K183408.
Who is the listed applicant for Jensen Shade Effect Liquids?
The FDA 510(k) record lists Jensen Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Jensen Shade Effect Liquids?
The FDA product code for Jensen Shade Effect Liquids is EIH.
相关临床试验
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相关器械（代码：EIH）
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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