Marie
K号: K250970 · 2025-07-25
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器械摘要
Marie is the device name listed in this FDA 510(k) record. The listed applicant is Leo Cancer Care. It received FDA 510(k) clearance on 2025-07-25 under 510(k) number K250970. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Marie?
Marie is a medical device that received FDA 510(k) clearance on 2025-07-25. The listed applicant is Leo Cancer Care. The 510(k) number is K250970.
When did Marie receive FDA 510(k) clearance?
Marie received FDA 510(k) clearance on 2025-07-25, under 510(k) number K250970.
Who is the listed applicant for Marie?
The FDA 510(k) record lists Leo Cancer Care as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Marie?
The FDA product code for Marie is JAK.
相关临床试验
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列明Leo Cancer Care为申报人的其他记录
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相关器械（代码：JAK）
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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官方来源
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