FDA 510(k)泰托体温计
K号: K190242 · 2019-03-27
决定日期2019-03-27
产品代码FLL
咨询委员会医疗设备监管文本翻译如下:
HO
请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同
器械摘要
Tyto Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Tyto Care , Ltd.. It received FDA 510(k) clearance on 2019-03-27 under 510(k) number K190242. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Tyto Thermometer?
Tyto Thermometer is a medical device that received FDA 510(k) clearance on 2019-03-27. The listed applicant is Tyto Care , Ltd.. The 510(k) number is K190242.
When did Tyto Thermometer receive FDA 510(k) clearance?
Tyto Thermometer received FDA 510(k) clearance on 2019-03-27, under 510(k) number K190242.
Who is the listed applicant for Tyto Thermometer?
The FDA 510(k) record lists Tyto Care , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tyto Thermometer?
The FDA product code for Tyto Thermometer is FLL.
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列明Tyto Care , Ltd.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。
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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。
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