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FDA 510(k)

RII 多功能红外线温度计,型号 TH52Z

K号: K162083 · 2017-01-09

决定日期2017-01-09
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

RII Multi-function Infrared Thermometer, Model TH52Z is the device name listed in this FDA 510(k) record. The listed applicant is Radiant Innovation, Inc.. It received FDA 510(k) clearance on 2017-01-09 under 510(k) number K162083. 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 RII Multi-function Infrared Thermometer, Model TH52Z?

RII Multi-function Infrared Thermometer, Model TH52Z is a medical device that received FDA 510(k) clearance on 2017-01-09. The listed applicant is Radiant Innovation, Inc.. The 510(k) number is K162083.

When did RII Multi-function Infrared Thermometer, Model TH52Z receive FDA 510(k) clearance?

RII Multi-function Infrared Thermometer, Model TH52Z received FDA 510(k) clearance on 2017-01-09, under 510(k) number K162083.

Who is the listed applicant for RII Multi-function Infrared Thermometer, Model TH52Z?

The FDA 510(k) record lists Radiant Innovation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RII Multi-function Infrared Thermometer, Model TH52Z?

The FDA product code for RII Multi-function Infrared Thermometer, Model TH52Z is FLL.

相关临床试验

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列明Radiant Innovation, Inc.为申报人的其他记录

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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。

官方来源

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