More-Cell-System
K号: K212659 · 2021-11-10
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决定日期2021-11-10
产品代码PMU
咨询委员会OB
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决定实质等同
器械摘要
More-Cell-System is the device name listed in this FDA 510(k) record. The listed applicant is Agency For Medical Innovations GmbH. It received FDA 510(k) clearance on 2021-11-10 under 510(k) number K212659. The device is classified under product code PMU. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the More-Cell-System?
More-Cell-System is a medical device that received FDA 510(k) clearance on 2021-11-10. The listed applicant is Agency For Medical Innovations GmbH. The 510(k) number is K212659.
When did More-Cell-System receive FDA 510(k) clearance?
More-Cell-System received FDA 510(k) clearance on 2021-11-10, under 510(k) number K212659.
Who is the listed applicant for More-Cell-System?
The FDA 510(k) record lists Agency For Medical Innovations GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for More-Cell-System?
The FDA product code for More-Cell-System is PMU.
相关临床试验
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列明Agency For Medical Innovations GmbH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：PMU）
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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