Non-contact Infrared Body Thermometer, model:HTD8823US
K-Number: K200159 · 2021-01-05
Device Summary
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.
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.