BD Alaris 系统带Guardrails Suite MX v12.1.2
K号: K211218 · 2023-07-21
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器械摘要
常见问题
What is the BD Alaris System with Guardrails Suite MX v12.1.2?
BD Alaris System with Guardrails Suite MX v12.1.2 is a medical device that received FDA 510(k) clearance on 2023-07-21. The listed applicant is Carefusion 303, Inc.. The 510(k) number is K211218.
When did BD Alaris System with Guardrails Suite MX v12.1.2 receive FDA 510(k) clearance?
BD Alaris System with Guardrails Suite MX v12.1.2 received FDA 510(k) clearance on 2023-07-21, under 510(k) number K211218.
Who is the listed applicant for BD Alaris System with Guardrails Suite MX v12.1.2?
The FDA 510(k) record lists Carefusion 303, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD Alaris System with Guardrails Suite MX v12.1.2?
The FDA product code for BD Alaris System with Guardrails Suite MX v12.1.2 is FRN.
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Carefusion 303, 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:FRN)
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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