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FDA 510(k)

紅外線非接觸式體溫計,型號 ACT8100

K 號:K162509 · 2017-03-10

決定日期2017-03-10
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 Non-contact Thermometer, Model ACT8100 is the device name listed in this FDA 510(k) record. The listed applicant is Easywell Biomedicals, Inc.. It received FDA 510(k) clearance on 2017-03-10 under 510(k) number K162509. 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 Non-contact Thermometer, Model ACT8100?

Infrared Non-contact Thermometer, Model ACT8100 is a medical device that received FDA 510(k) clearance on 2017-03-10. The listed applicant is Easywell Biomedicals, Inc.. The 510(k) number is K162509.

When did Infrared Non-contact Thermometer, Model ACT8100 receive FDA 510(k) clearance?

Infrared Non-contact Thermometer, Model ACT8100 received FDA 510(k) clearance on 2017-03-10, under 510(k) number K162509.

Who is the listed applicant for Infrared Non-contact Thermometer, Model ACT8100?

The FDA 510(k) record lists Easywell Biomedicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Infrared Non-contact Thermometer, Model ACT8100?

The FDA product code for Infrared Non-contact Thermometer, Model ACT8100 is FLL.

相關臨床試驗

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其他以 Easywell Biomedicals, Inc. 為申請人之記錄

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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。

官方來源

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