BD Vacutainer® 多样本 Luer 适配器
K号: K243649 · 2025-03-21
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器械摘要
常见问题
What is the BD Vacutainer® Multiple Sample Luer Adapter?
BD Vacutainer® Multiple Sample Luer Adapter is a medical device that received FDA 510(k) clearance on 2025-03-21. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K243649.
When did BD Vacutainer® Multiple Sample Luer Adapter receive FDA 510(k) clearance?
BD Vacutainer® Multiple Sample Luer Adapter received FDA 510(k) clearance on 2025-03-21, under 510(k) number K243649.
Who is the listed applicant for BD Vacutainer® Multiple Sample Luer Adapter?
The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD Vacutainer® Multiple Sample Luer Adapter?
The FDA product code for BD Vacutainer® Multiple Sample Luer Adapter is JKA.
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Becton, Dickinson and Company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:JKA)
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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