Mosie Baby Kit
K号: K231203 · 2023-11-29
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申请人Mosie Baby
决定日期2023-11-29
产品代码QYZ
咨询委员会OB
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决定实质等同
器械摘要
Mosie Baby Kit is the device name listed in this FDA 510(k) record. The listed applicant is Mosie Baby. It received FDA 510(k) clearance on 2023-11-29 under 510(k) number K231203. The device is classified under product code QYZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Mosie Baby Kit?
Mosie Baby Kit is a medical device that received FDA 510(k) clearance on 2023-11-29. The listed applicant is Mosie Baby. The 510(k) number is K231203.
When did Mosie Baby Kit receive FDA 510(k) clearance?
Mosie Baby Kit received FDA 510(k) clearance on 2023-11-29, under 510(k) number K231203.
Who is the listed applicant for Mosie Baby Kit?
The FDA 510(k) record lists Mosie Baby as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Mosie Baby Kit?
The FDA product code for Mosie Baby Kit is QYZ.
相关临床试验
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相关器械（代码：QYZ）
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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