DT-100
K号: K160358 · 2017-02-24
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决定日期2017-02-24
产品代码FLL
咨询委员会医疗设备监管文本翻译如下：
HO
请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同
器械摘要
DT-100 is the device name listed in this FDA 510(k) record. The listed applicant is Mediana Co., Ltd.. It received FDA 510(k) clearance on 2017-02-24 under 510(k) number K160358. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DT-100?
DT-100 is a medical device that received FDA 510(k) clearance on 2017-02-24. The listed applicant is Mediana Co., Ltd.. The 510(k) number is K160358.
When did DT-100 receive FDA 510(k) clearance?
DT-100 received FDA 510(k) clearance on 2017-02-24, under 510(k) number K160358.
Who is the listed applicant for DT-100?
The FDA 510(k) record lists Mediana Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DT-100?
The FDA product code for DT-100 is FLL.
列明Mediana Co., Ltd.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：FLL）
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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