湿信 D2care
K号: K170797 · 2017-12-06
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决定日期2017-12-06
产品代码NUC
咨询委员会OB
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决定实质等同
器械摘要
wettrust D2care is the device name listed in this FDA 510(k) record. The listed applicant is Wettrust Korea Co., Ltd.. It received FDA 510(k) clearance on 2017-12-06 under 510(k) number K170797. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the wettrust D2care?
wettrust D2care is a medical device that received FDA 510(k) clearance on 2017-12-06. The listed applicant is Wettrust Korea Co., Ltd.. The 510(k) number is K170797.
When did wettrust D2care receive FDA 510(k) clearance?
wettrust D2care received FDA 510(k) clearance on 2017-12-06, under 510(k) number K170797.
Who is the listed applicant for wettrust D2care?
The FDA 510(k) record lists Wettrust Korea Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for wettrust D2care?
The FDA product code for wettrust D2care is NUC.
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：NUC）
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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