紅外線體溫計
K 號：K200781 · 2020-12-09
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決定日期2020-12-09
產品代碼FLL
諮詢委員會醫療設備規範文本翻譯如下：
HO
注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於
器材摘要
Infrared Body Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Heitaida Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-12-09 under 510(k) number K200781. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Infrared Body Thermometer?
Infrared Body Thermometer is a medical device that received FDA 510(k) clearance on 2020-12-09. The listed applicant is Heitaida Technology Co., Ltd.. The 510(k) number is K200781.
When did Infrared Body Thermometer receive FDA 510(k) clearance?
Infrared Body Thermometer received FDA 510(k) clearance on 2020-12-09, under 510(k) number K200781.
Who is the listed applicant for Infrared Body Thermometer?
The FDA 510(k) record lists Heitaida Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Infrared Body Thermometer?
The FDA product code for Infrared Body Thermometer is FLL.
相關臨床試驗
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
相關器械（代碼：FLL）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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