免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

红外额温计,红外耳/额温计

K号: K181239 · 2018-10-29

决定日期2018-10-29
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

Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Joytech Healthcare Co. , Ltd.. It received FDA 510(k) clearance on 2018-10-29 under 510(k) number K181239. 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 Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer?

Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer is a medical device that received FDA 510(k) clearance on 2018-10-29. The listed applicant is Joytech Healthcare Co. , Ltd.. The 510(k) number is K181239.

When did Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer receive FDA 510(k) clearance?

Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer received FDA 510(k) clearance on 2018-10-29, under 510(k) number K181239.

Who is the listed applicant for Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer?

FDA 510(k)记录将Joytech Healthcare Co., Ltd.列为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Infrared Forehead Thermometer, Infrared Ear/Forehead Thermometer?

The FDA product code for Infrared Forehead Thermometer, Infrared Ear/Forehead 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Joytech Healthcare Co. , 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。

查看所有 24 个设备 →

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。

↑