“MoFi”细胞培养基础培养基
K号: K240247 · 2024-07-12
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决定日期2024-07-12
产品代码NDS
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定实质等同
器械摘要
“MoFi” Cell Culture Basal Medium is the device name listed in this FDA 510(k) record. The listed applicant is Duogenic Stemcells Corporation. It received FDA 510(k) clearance on 2024-07-12 under 510(k) number K240247. The device is classified under product code NDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the “MoFi” Cell Culture Basal Medium?
“MoFi” Cell Culture Basal Medium is a medical device that received FDA 510(k) clearance on 2024-07-12. The listed applicant is Duogenic Stemcells Corporation. The 510(k) number is K240247.
When did “MoFi” Cell Culture Basal Medium receive FDA 510(k) clearance?
“MoFi” Cell Culture Basal Medium received FDA 510(k) clearance on 2024-07-12, under 510(k) number K240247.
Who is the listed applicant for “MoFi” Cell Culture Basal Medium?
The FDA 510(k) record lists Duogenic Stemcells Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for “MoFi” Cell Culture Basal Medium?
The FDA product code for “MoFi” Cell Culture Basal Medium is NDS.
相关临床试验
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相关器械（代码：NDS）
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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