MDT2 蓝牙自监测血糖系统
K号: K190189 · 2019-11-01
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器械摘要
常见问题
What is the MDT2 BLE Self-Monitoring Blood Glucose System?
MDT2 BLE Self-Monitoring Blood Glucose System is a medical device that received FDA 510(k) clearance on 2019-11-01. The listed applicant is Eps Bio Technology Corp.. The 510(k) number is K190189.
When did MDT2 BLE Self-Monitoring Blood Glucose System receive FDA 510(k) clearance?
MDT2 BLE Self-Monitoring Blood Glucose System received FDA 510(k) clearance on 2019-11-01, under 510(k) number K190189.
Who is the listed applicant for MDT2 BLE Self-Monitoring Blood Glucose System?
The FDA 510(k) record lists Eps Bio Technology Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MDT2 BLE Self-Monitoring Blood Glucose System?
The FDA product code for MDT2 BLE Self-Monitoring Blood Glucose System is NBW. This falls under the OB/GYN category.
相关临床试验
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列明Eps Bio Technology Corp.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:NBW)
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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