MS Lide植入系统
K号: K181477 · 2020-10-20
广告
决定日期2020-10-20
产品代码DZE
咨询委员会DE
请注意，您没有提供具体的医疗设备监管文本内容，因此我无法进行翻译。请提供需要翻译的具体文本，我将根据您的要求进行翻译。
决定实质等同
器械摘要
MS Lide Implant Systems is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-10-20 under 510(k) number K181477. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MS Lide Implant Systems?
MS Lide Implant Systems is a medical device that received FDA 510(k) clearance on 2020-10-20. The listed applicant is Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.. The 510(k) number is K181477.
When did MS Lide Implant Systems receive FDA 510(k) clearance?
MS Lide Implant Systems received FDA 510(k) clearance on 2020-10-20, under 510(k) number K181477.
Who is the listed applicant for MS Lide Implant Systems?
The FDA 510(k) record lists Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MS Lide Implant Systems?
The FDA product code for MS Lide Implant Systems is DZE.
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：DZE）
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。
广告