Vicks VNT200 No Touch Forehead Thermometer
K-Number: K193213 · 2020-04-28
Device Summary
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. 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.
Other records listing Kaz USA, Inc., A Helen of Troy Company as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FLL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.