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FDA 510(k)

ARTSMedia 卵母细胞吸取介质 (502020, 502050, 502100)

K号: K241132 · 2024-12-18

决定日期2024-12-18
产品代码MQL
咨询委员会OB 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100) is the device name listed in this FDA 510(k) record. The listed applicant is Artsmedia Denmark Aps. It received FDA 510(k) clearance on 2024-12-18 under 510(k) number K241132. 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 ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100)?

ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100) is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is Artsmedia Denmark Aps. The 510(k) number is K241132.

When did ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100) receive FDA 510(k) clearance?

ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100) received FDA 510(k) clearance on 2024-12-18, under 510(k) number K241132.

Who is the listed applicant for ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100)?

The FDA 510(k) record lists Artsmedia Denmark Aps as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100)?

The FDA product code for ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100) is MQL.

相关临床试验

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。

列明Artsmedia Denmark Aps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: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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