LifeSignals WiPoint 生物传感器_iOS 接收器_应用程序系统(LifeSignals WiPatch & WiApp 系统)
K号: K172011 · 2018-06-14
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器械摘要
常见问题
What is the LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)?
LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) is a medical device that received FDA 510(k) clearance on 2018-06-14. The listed applicant is Hmicro, Inc.. The 510(k) number is K172011.
When did LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) receive FDA 510(k) clearance?
LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) received FDA 510(k) clearance on 2018-06-14, under 510(k) number K172011.
Who is the listed applicant for LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)?
The FDA 510(k) record lists Hmicro, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)?
The FDA product code for LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) 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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