Cleared Traditional

K200946 - Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) (FDA 510(k) Clearance)

Apr 2022
Decision
727d
Days
Class 2
Risk

K200946 is an FDA 510(k) clearance for the Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241). This device is classified as a Continuous Measurement Thermometer (Class II - Special Controls, product code FLL).

Submitted by Taidoc Technology Corporation (New Taipei City, TW). The FDA issued a Cleared decision on April 5, 2022, 727 days after receiving the submission on April 8, 2020.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.2910. A Continuous Measurement Thermometer Is A Clinical Electronic Thermometer Indicated To Measure The Body Or Skin Temperature Of A Person Continuously Or In Specified Intervals. Under This Regulation, This Product Code Represents Non-exempt Devices. For More Information, See 90 Fr 25889, Available At Https://www.govinfo.gov/content/pkg/fr-2025-06-18/pdf/2025-11207.pdf..

Submission Details

510(k) Number K200946 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 08, 2020
Decision Date April 05, 2022
Days to Decision 727 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FLL — Continuous Measurement Thermometer
Device Class Class II - Special Controls
CFR Regulation 21 CFR 880.2910
Definition A Continuous Measurement Thermometer Is A Clinical Electronic Thermometer Indicated To Measure The Body Or Skin Temperature Of A Person Continuously Or In Specified Intervals. Under This Regulation, This Product Code Represents Non-exempt Devices. For More Information, See 90 Fr 25889, Available At Https://www.govinfo.gov/content/pkg/fr-2025-06-18/pdf/2025-11207.pdf.

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