BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit
K号: K232434 · 2023-12-05
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器械摘要
常见问题
What is the BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit?
BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit is a medical device that received FDA 510(k) clearance on 2023-12-05. The listed applicant is Bd. The 510(k) number is K232434.
When did BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit receive FDA 510(k) clearance?
BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit received FDA 510(k) clearance on 2023-12-05, under 510(k) number K232434.
Who is the listed applicant for BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit?
The FDA 510(k) record lists Bd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit?
The FDA product code for BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit is PSZ.
相关临床试验
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列明Bd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:PSZ)
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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