LS OIL
K号: K173920 · 2018-10-11
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决定日期2018-10-11
产品代码EKX
咨询委员会DE
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决定实质等同
器械摘要
LS OIL is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2018-10-11 under 510(k) number K173920. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LS OIL?
LS OIL is a medical device that received FDA 510(k) clearance on 2018-10-11. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K173920.
When did LS OIL receive FDA 510(k) clearance?
LS OIL received FDA 510(k) clearance on 2018-10-11, under 510(k) number K173920.
Who is the listed applicant for LS OIL?
The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LS OIL?
The FDA product code for LS OIL is EKX.
列明J. Morita USA, 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：EKX）
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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