LifeStream管理系统，LifeStream管理套件，LifeStream患者管理器，LifeStream管理器，LifeStream网络管理器，LifeStream
K号: K153719 · 2016-06-03
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器械摘要
常见问题
What is the LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream?
LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream is a medical device that received FDA 510(k) clearance on 2016-06-03. The listed applicant is Honeywell Hommed, LLC. The 510(k) number is K153719.
When did LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream receive FDA 510(k) clearance?
LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream received FDA 510(k) clearance on 2016-06-03, under 510(k) number K153719.
Who is the listed applicant for LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream?
The FDA 510(k) record lists Honeywell Hommed, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream?
The FDA product code for LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream is DRG.
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。
相关器械（代码：DRG）
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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