FDA 510(k)

Vicks VNT200 No Touch Forehead Thermometer

Número K: K193213 · 2020-04-28

RequerenteKaz USA, Inc., A Helen of Troy Company

Data da decisão2020-04-28

Código do produtoFLL

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vicks VNT200 No Touch Forehead Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Kaz USA, Inc., A Helen of Troy Company. It received FDA 510(k) clearance on 2020-04-28 under 510(k) number K193213. 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 Vicks VNT200 No Touch Forehead Thermometer?

Vicks VNT200 No Touch Forehead Thermometer is a medical device that received FDA 510(k) clearance on 2020-04-28. The listed applicant is Kaz USA, Inc., A Helen of Troy Company. The 510(k) number is K193213.

When did Vicks VNT200 No Touch Forehead Thermometer receive FDA 510(k) clearance?

Vicks VNT200 No Touch Forehead Thermometer received FDA 510(k) clearance on 2020-04-28, under 510(k) number K193213.

Who is the listed applicant for Vicks VNT200 No Touch Forehead Thermometer?

The FDA 510(k) record lists Kaz USA, Inc., A Helen of Troy Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vicks VNT200 No Touch Forehead Thermometer?

The FDA product code for Vicks VNT200 No Touch Forehead Thermometer is FLL.

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Outros registros que listam Kaz USA, Inc., A Helen of Troy Company como candidato(a)

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Dispositivos Relacionados (Código: FLL)

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Fonte oficial

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