Infrared Forehead Thermometer
K-Number: K220084 · 2022-09-12
Decision Date2022-09-12
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Infrared Forehead Thermometer is a medical device manufactured by Qingdao Yasee Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2022-09-12 under approval number K220084. 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 Forehead Thermometer?
Infrared Forehead Thermometer is a medical device that received FDA 510(k) clearance on 2022-09-12. It is manufactured by Qingdao Yasee Medical Device Co., Ltd.. The 510(k) number is K220084.
When was Infrared Forehead Thermometer approved by the FDA?
Infrared Forehead Thermometer received FDA 510(k) clearance on 2022-09-12, under approval number K220084.
What company makes Infrared Forehead Thermometer?
Infrared Forehead Thermometer is manufactured by Qingdao Yasee Medical Device Co., Ltd..
What is the FDA product code for Infrared Forehead Thermometer?
The FDA product code for Infrared Forehead Thermometer is FLL.
Related Clinical Trials
Other Devices by Qingdao Yasee Medical Device Co., Ltd.
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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.