Welch Allyn Connex® 即时监测仪;901058 生命体征监测仪核心(CSM)
K号: K241411 · 2024-12-20
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器械摘要
常见问题
What is the Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)?
Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM) is a medical device that received FDA 510(k) clearance on 2024-12-20. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K241411.
When did Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM) receive FDA 510(k) clearance?
Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM) received FDA 510(k) clearance on 2024-12-20, under 510(k) number K241411.
Who is the listed applicant for Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)?
The FDA 510(k) record lists Welch Allyn, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)?
The FDA product code for Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM) is MWI.
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Welch Allyn, 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:MWI)
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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