SSS-NX(血清替代补充-NX)
K号: K233764 · 2024-04-24
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器械摘要
常见问题
What is the SSS-NX (Serum Substitute Supplement-NX)?
SSS-NX (Serum Substitute Supplement-NX) is a medical device that received FDA 510(k) clearance on 2024-04-24. The listed applicant is Fujifilm Irvine Scientific. The 510(k) number is K233764.
When did SSS-NX (Serum Substitute Supplement-NX) receive FDA 510(k) clearance?
SSS-NX (Serum Substitute Supplement-NX) received FDA 510(k) clearance on 2024-04-24, under 510(k) number K233764.
Who is the listed applicant for SSS-NX (Serum Substitute Supplement-NX)?
The FDA 510(k) record lists Fujifilm Irvine Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SSS-NX (Serum Substitute Supplement-NX)?
The FDA product code for SSS-NX (Serum Substitute Supplement-NX) is MQL.
相关临床试验
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列明Fujifilm Irvine Scientific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
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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