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FDA 510(k)

Vicks VNT200 No Touch Forehead Thermometer

K-Number: K193213 · 2020-04-28

Decision Date2020-04-28
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

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

When was Vicks VNT200 No Touch Forehead Thermometer approved by the FDA?

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

What company makes Vicks VNT200 No Touch Forehead Thermometer?

Vicks VNT200 No Touch Forehead Thermometer is manufactured by Kaz USA, Inc., A Helen of Troy Company.

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.

Other Devices by Kaz USA, Inc., A Helen of Troy Company

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Related Devices (Code: FLL)

Official Source

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