AnyCheck IMT-100
K号: K180953 · 2019-02-20
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决定日期2019-02-20
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
AnyCheck IMT-100 is the device name listed in this FDA 510(k) record. The listed applicant is Dms Co., Ltd.. It received FDA 510(k) clearance on 2019-02-20 under 510(k) number K180953. 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 AnyCheck IMT-100?
AnyCheck IMT-100 is a medical device that received FDA 510(k) clearance on 2019-02-20. The listed applicant is Dms Co., Ltd.. The 510(k) number is K180953.
When did AnyCheck IMT-100 receive FDA 510(k) clearance?
AnyCheck IMT-100 received FDA 510(k) clearance on 2019-02-20, under 510(k) number K180953.
Who is the listed applicant for AnyCheck IMT-100?
The FDA 510(k) record lists Dms Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AnyCheck IMT-100?
The FDA product code for AnyCheck IMT-100 is EKX.
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。
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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