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FDA 510(k)

Non-contact Infrared Body Thermometer, model:HTD8823US

K-Number: K200159 · 2021-01-05

Decision Date2021-01-05
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Non-contact Infrared Body Thermometer, model:HTD8823US is the device name listed in this FDA 510(k) record. The listed applicant is Hetaida Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-01-05 under 510(k) number K200159. 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 Non-contact Infrared Body Thermometer, model:HTD8823US?

Non-contact Infrared Body Thermometer, model:HTD8823US is a medical device that received FDA 510(k) clearance on 2021-01-05. The listed applicant is Hetaida Technology Co., Ltd.. The 510(k) number is K200159.

When did Non-contact Infrared Body Thermometer, model:HTD8823US receive FDA 510(k) clearance?

Non-contact Infrared Body Thermometer, model:HTD8823US received FDA 510(k) clearance on 2021-01-05, under 510(k) number K200159.

Who is the listed applicant for Non-contact Infrared Body Thermometer, model:HTD8823US?

The FDA 510(k) record lists Hetaida Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Non-contact Infrared Body Thermometer, model:HTD8823US?

The FDA product code for Non-contact Infrared Body Thermometer, model:HTD8823US is FLL.

Related Clinical Trials

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.

Other records listing Hetaida Technology Co., Ltd. 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.

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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.