I Do
K号: K192294 · 2020-07-31
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决定日期2020-07-31
产品代码DZE
咨询委员会DE
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决定实质等同
器械摘要
I Do is the device name listed in this FDA 510(k) record. The listed applicant is I DO Biotech Co., Ltd.. It received FDA 510(k) clearance on 2020-07-31 under 510(k) number K192294. 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 I Do?
I Do is a medical device that received FDA 510(k) clearance on 2020-07-31. The listed applicant is I DO Biotech Co., Ltd.. The 510(k) number is K192294.
When did I Do receive FDA 510(k) clearance?
I Do received FDA 510(k) clearance on 2020-07-31, under 510(k) number K192294.
Who is the listed applicant for I Do?
The FDA 510(k) record lists I DO Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for I Do?
The FDA product code for I Do is DZE.
相关器械（代码：DZE）
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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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