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FDA 510(k)

Mon-a-Therm®通用温度探头400TM(90050, 90044)

K号: K240077 · 2024-08-20

申请人Covidien
决定日期2024-08-20
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

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2024-08-20 under 510(k) number K240077. 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 Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)?

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) is a medical device that received FDA 510(k) clearance on 2024-08-20. The listed applicant is Covidien. The 510(k) number is K240077.

When did Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) receive FDA 510(k) clearance?

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) received FDA 510(k) clearance on 2024-08-20, under 510(k) number K240077.

Who is the listed applicant for Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)?

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

What is the FDA product code for Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)?

The FDA product code for Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) is FLL.

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列明Covidien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。

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