FDA 510(k)

Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60

Número K: K202687 · 2021-02-18

RequerenteShenzhen Lepu Intelligent Medical Equipment Co., Ltd.

Data da decisão2021-02-18

Código do produtoFLL

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60 is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Lepu Intelligent Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2021-02-18 under 510(k) number K202687. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60?

Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60 is a medical device that received FDA 510(k) clearance on 2021-02-18. The listed applicant is Shenzhen Lepu Intelligent Medical Equipment Co., Ltd.. The 510(k) number is K202687.

When did Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60 receive FDA 510(k) clearance?

Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60 received FDA 510(k) clearance on 2021-02-18, under 510(k) number K202687.

Who is the listed applicant for Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60?

The FDA 510(k) record lists Shenzhen Lepu Intelligent Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60?

The FDA product code for Infrared Forehead Thermometer, Model LFR30B, LFR50, LFR60 is FLL.

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Dispositivos Relacionados (Código: FLL)

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Fonte oficial

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