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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 the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2022-04-05 under 510(k) 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. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K200946.

When did Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241) receive FDA 510(k) clearance?

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

Who is the listed applicant for Clever Forehead Thermometer / Clever Medical Forehead Thermometer (Model TD-1241)?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Taidoc Technology Corporation 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.

View all 17 devices →

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

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