DIAZIR
K号: K161652 · 2017-11-28
广告
决定日期2017-11-28
产品代码EIH
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
DIAZIR is the device name listed in this FDA 510(k) record. The listed applicant is Zxtgy (Beijing) Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-11-28 under 510(k) number K161652. 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 DIAZIR?
DIAZIR is a medical device that received FDA 510(k) clearance on 2017-11-28. The listed applicant is Zxtgy (Beijing) Technology Co., Ltd.. The 510(k) number is K161652.
When did DIAZIR receive FDA 510(k) clearance?
DIAZIR received FDA 510(k) clearance on 2017-11-28, under 510(k) number K161652.
Who is the listed applicant for DIAZIR?
The FDA 510(k) record lists Zxtgy (Beijing) Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAZIR?
The FDA product code for DIAZIR is EIH.
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：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。
广告