F1 Mothership 无线传感器，用于胎儿超声和多普勒监测
K号: K171865 · 2017-08-24
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器械摘要
常见问题
What is the F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring?
F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring is a medical device that received FDA 510(k) clearance on 2017-08-24. The listed applicant is Farus, LLC. The 510(k) number is K171865.
When did F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring receive FDA 510(k) clearance?
F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring received FDA 510(k) clearance on 2017-08-24, under 510(k) number K171865.
Who is the listed applicant for F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring?
The FDA 510(k) record lists Farus, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring?
The FDA product code for F1 Mothership Wireless Transducers for Fetal Ultrasonic and Tocodynamometer Monitoring is HGM.
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：HGM）
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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