MOZI TPS
K号: K223724 · 2023-07-10
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器械摘要
MOZI TPS is the device name listed in this FDA 510(k) record. The listed applicant is Manteia Technologies Co., Ltd.. It received FDA 510(k) clearance on 2023-07-10 under 510(k) number K223724. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MOZI TPS?
MOZI TPS is a medical device that received FDA 510(k) clearance on 2023-07-10. The listed applicant is Manteia Technologies Co., Ltd.. The 510(k) number is K223724.
When did MOZI TPS receive FDA 510(k) clearance?
MOZI TPS received FDA 510(k) clearance on 2023-07-10, under 510(k) number K223724.
Who is the listed applicant for MOZI TPS?
FDA 510(k)记录将Manteia Technologies Co., Ltd.列为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for MOZI TPS?
The FDA product code for MOZI TPS is MUJ.
列明Manteia Technologies Co., Ltd.为申报人的其他记录
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：MUJ）
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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