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FDA 510(k)

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)

K-Number: K240077 · 2024-08-20

ApplicantCovidien
Decision Date2024-08-20
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) is a medical device manufactured by Covidien. It received FDA 510(k) clearance on 2024-08-20 under approval number K240077. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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. It is manufactured by Covidien. The 510(k) number is K240077.

When was Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) approved by the FDA?

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

What company makes Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)?

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) is manufactured by Covidien.

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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Related Devices (Code: FLL)

K160306Cloud Smart ThermometerGuangzhou Bosma Technology Co, Ltd. K161728Microlife Digital Infrared Forehead Thermometer, Model FR1MN1-1Microfile Intellectual Property GmbH K161735Non-contact Forehead ThermometerShenzhen Dongdixin Technology Co., Ltd. K160816Infrared Thermometer (Model: LX-26E, LX-260TE, PRO LX-261E, LX-360, LX-361T, BW-CX10)Nexmed Technology Co., Ltd. K161211Digital ThermometerBiocare Asia Corporation , Ltd. K160802Infrared Forehead Thermometer, FT-100AHangzhou Universal Electronic Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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