BD Vacutainer® 单次使用夹持器
K号: K242320 · 2024-11-01
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器械摘要
常见问题
What is the BD Vacutainer® One Use Holder?
BD Vacutainer® One Use Holder is a medical device that received FDA 510(k) clearance on 2024-11-01. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K242320.
When did BD Vacutainer® One Use Holder receive FDA 510(k) clearance?
BD Vacutainer® One Use Holder received FDA 510(k) clearance on 2024-11-01, under 510(k) number K242320.
Who is the listed applicant for BD Vacutainer® One Use Holder?
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® One Use Holder?
The FDA product code for BD Vacutainer® One Use Holder 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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