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FDA 510(k)

红外温度计 TET-351

K号: K220276 · 2023-02-17

决定日期2023-02-17
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 Thermometer TET-351 is the device name listed in this FDA 510(k) record. The listed applicant is Truly Instrument Limited. It received FDA 510(k) clearance on 2023-02-17 under 510(k) number K220276. 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 Thermometer TET-351?

Infrared Thermometer TET-351 is a medical device that received FDA 510(k) clearance on 2023-02-17. The listed applicant is Truly Instrument Limited. The 510(k) number is K220276.

When did Infrared Thermometer TET-351 receive FDA 510(k) clearance?

Infrared Thermometer TET-351 received FDA 510(k) clearance on 2023-02-17, under 510(k) number K220276.

Who is the listed applicant for Infrared Thermometer TET-351?

The FDA 510(k) record lists Truly Instrument Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Infrared Thermometer TET-351?

The FDA product code for Infrared Thermometer TET-351 is FLL.

相关临床试验

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列明Truly Instrument Limited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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