瑞福美预测式体温计
K号: K171182 · 2017-10-04
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器械摘要
常见问题
What is the ri-former Predictive Thermometer?
ri-former Predictive Thermometer is a medical device that received FDA 510(k) clearance on 2017-10-04. The listed applicant is Rudolf Riester GmbH. The 510(k) number is K171182.
When did ri-former Predictive Thermometer receive FDA 510(k) clearance?
ri-former Predictive Thermometer received FDA 510(k) clearance on 2017-10-04, under 510(k) number K171182.
Who is the listed applicant for ri-former Predictive Thermometer?
The FDA 510(k) record lists Rudolf Riester GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ri-former Predictive Thermometer?
The FDA product code for ri-former Predictive Thermometer 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。
列明Rudolf Riester GmbH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: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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