Gold Standard Diagnostics (GSD) AIX1000 快速血浆反应素(RPR)自动测试系统
K号: K250249 · 2025-10-10
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器械摘要
常见问题
What is the Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System?
Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System is a medical device that received FDA 510(k) clearance on 2025-10-10. The listed applicant is Gold Standard Diagnostics, LLC. The 510(k) number is K250249.
When did Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System receive FDA 510(k) clearance?
Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System received FDA 510(k) clearance on 2025-10-10, under 510(k) number K250249.
Who is the listed applicant for Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System?
The FDA 510(k) record lists Gold Standard Diagnostics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System?
The FDA product code for Gold Standard Diagnostics (GSD) AIX1000 Rapid Plasma Reagin (RPR) Automated Test System is GMQ.
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。
相关器械(代码:GMQ)
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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