Swaive 體溫計 SWT1A
K 號：K170723 · 2018-10-25
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決定日期2018-10-25
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
Swaive Thermometer SWT1A is the device name listed in this FDA 510(k) record. The listed applicant is E-Care Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-10-25 under 510(k) number K170723. 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 Swaive Thermometer SWT1A?
Swaive Thermometer SWT1A is a medical device that received FDA 510(k) clearance on 2018-10-25. The listed applicant is E-Care Technology Co., Ltd.. The 510(k) number is K170723.
When did Swaive Thermometer SWT1A receive FDA 510(k) clearance?
Swaive Thermometer SWT1A received FDA 510(k) clearance on 2018-10-25, under 510(k) number K170723.
Who is the listed applicant for Swaive Thermometer SWT1A?
The FDA 510(k) record lists E-Care Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Swaive Thermometer SWT1A?
The FDA product code for Swaive Thermometer SWT1A is FLL.
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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。
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官方來源
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