红外温度计,Breeze 型号
K号: K191283 · 2019-10-18
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器械摘要
常见问题
What is the Infrared Thermometer, Breeze model?
Infrared Thermometer, Breeze model is a medical device that received FDA 510(k) clearance on 2019-10-18. The listed applicant is Suzhou Melodicare Medical Technology Co., Ltd.. The 510(k) number is K191283.
When did Infrared Thermometer, Breeze model receive FDA 510(k) clearance?
Infrared Thermometer, Breeze model received FDA 510(k) clearance on 2019-10-18, under 510(k) number K191283.
Who is the listed applicant for Infrared Thermometer, Breeze model?
The FDA 510(k) record lists Suzhou Melodicare Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Infrared Thermometer, Breeze model?
The FDA product code for Infrared Thermometer, Breeze model is FLL.
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:FLL)
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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