cobas® SARS-CoV-2 定性检测,适用于cobas® 5800/6800/8800 系统
K号: K240867 · 2025-02-11
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器械摘要
常见问题
What is the cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems?
cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems is a medical device that received FDA 510(k) clearance on 2025-02-11. The listed applicant is Roche Molecular Systems, Inc.. The 510(k) number is K240867.
When did cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems receive FDA 510(k) clearance?
cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems received FDA 510(k) clearance on 2025-02-11, under 510(k) number K240867.
Who is the listed applicant for cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems?
FDA 510(k)记录中列出罗氏分子系统有限公司为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems?
The FDA product code for cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems is QQX.
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Roche Molecular Systems, Inc.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:QQX)
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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