D功能
K号: K203525 · 2021-05-05
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决定日期2021-05-05
产品代码NUW
咨询委员会PM
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决定实质等同
器械摘要
D function is the device name listed in this FDA 510(k) record. The listed applicant is Ito Co., Ltd.. It received FDA 510(k) clearance on 2021-05-05 under 510(k) number K203525. The device is classified under product code NUW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the D function?
D function is a medical device that received FDA 510(k) clearance on 2021-05-05. The listed applicant is Ito Co., Ltd.. The 510(k) number is K203525.
When did D function receive FDA 510(k) clearance?
D function received FDA 510(k) clearance on 2021-05-05, under 510(k) number K203525.
Who is the listed applicant for D function?
The FDA 510(k) record lists Ito Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for D function?
The FDA product code for D function is NUW.
相关临床试验
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相关器械（代码：NUW）
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。
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