ClearLLab 10C 面板(B,T,M1,M2),Navios 流式细胞仪,Navios EX 流式细胞仪
K号: K183592 · 2019-03-21
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器械摘要
常见问题
What is the ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer?
ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer is a medical device that received FDA 510(k) clearance on 2019-03-21. The listed applicant is Beckman Coulter. The 510(k) number is K183592.
When did ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer receive FDA 510(k) clearance?
ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer received FDA 510(k) clearance on 2019-03-21, under 510(k) number K183592.
Who is the listed applicant for ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer?
The FDA 510(k) record lists Beckman Coulter as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer?
The FDA product code for ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer is PWD.
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Beckman Coulter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。
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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