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FDA 510(k)

Infrared Thermometer

K-Number: K180314 · 2018-07-11

ApplicantXuzhou Yongkang Electronic Science Technology Co., Ltd.
Decision Date2018-07-11
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Infrared Thermometer is a medical device manufactured by Xuzhou Yongkang Electronic Science Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-07-11 under approval number K180314. 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 Infrared Thermometer?

Infrared Thermometer is a medical device that received FDA 510(k) clearance on 2018-07-11. It is manufactured by Xuzhou Yongkang Electronic Science Technology Co., Ltd.. The 510(k) number is K180314.

When was Infrared Thermometer approved by the FDA?

Infrared Thermometer received FDA 510(k) clearance on 2018-07-11, under approval number K180314.

What company makes Infrared Thermometer?

Infrared Thermometer is manufactured by Xuzhou Yongkang Electronic Science Technology Co., Ltd..

What is the FDA product code for Infrared Thermometer?

The FDA product code for Infrared Thermometer is FLL.

Other Devices by Xuzhou Yongkang Electronic Science Technology Co., Ltd.

K161938Fingertip Pulse Oximeter K162616Wrist Type Blood Pressure Monitor K183491Arm Blood Pressure Monitor K191571UV Radiation Treatment System K252709Wireless Probe Type Ultrasound Scanner

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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