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FDA 510(k)

卵母细胞冲洗与采集介质;配子缓冲液

K号: K234023 · 2024-05-10

决定日期2024-05-10
产品代码MQL
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决定实质等同

器械摘要

Oocyte Flushing & Retrieval Medium; Gamete Buffer is the device name listed in this FDA 510(k) record. The listed applicant is Gimbo Medical Technology Shenzhen Co., Ltd.. It received FDA 510(k) clearance on 2024-05-10 under 510(k) number K234023. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Oocyte Flushing & Retrieval Medium; Gamete Buffer?

Oocyte Flushing & Retrieval Medium; Gamete Buffer is a medical device that received FDA 510(k) clearance on 2024-05-10. The listed applicant is Gimbo Medical Technology Shenzhen Co., Ltd.. The 510(k) number is K234023.

When did Oocyte Flushing & Retrieval Medium; Gamete Buffer receive FDA 510(k) clearance?

Oocyte Flushing & Retrieval Medium; Gamete Buffer received FDA 510(k) clearance on 2024-05-10, under 510(k) number K234023.

Who is the listed applicant for Oocyte Flushing & Retrieval Medium; Gamete Buffer?

The FDA 510(k) record lists Gimbo Medical Technology Shenzhen Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Oocyte Flushing & Retrieval Medium; Gamete Buffer?

The FDA product code for Oocyte Flushing & Retrieval Medium; Gamete Buffer is MQL.

相关临床试验

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列明Gimbo Medical Technology Shenzhen 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。

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相关器械(代码:MQL)

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

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