Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241)

K-Number: K200946 · 2022-04-05

Decision Date2022-04-05
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) is a medical device manufactured by Taidoc Technology Corporation. It received FDA 510(k) clearance on 2022-04-05 under approval number K200946. 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 Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241)?

Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) is a medical device that received FDA 510(k) clearance on 2022-04-05. It is manufactured by Taidoc Technology Corporation. The 510(k) number is K200946.

When was Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) approved by the FDA?

Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) received FDA 510(k) clearance on 2022-04-05, under approval number K200946.

What company makes Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241)?

Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) is manufactured by Taidoc Technology Corporation.

What is the FDA product code for Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241)?

The FDA product code for Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) is FLL.

Related Clinical Trials

Related PubMed Literature

Other Devices by Taidoc Technology Corporation

View all 17 devices →

Related Devices (Code: FLL)

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.