互動熱像儀
K 號：K181716 · 2019-03-25
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決定日期2019-03-25
產品代碼LHQ
諮詢委員會OB設備之醫療設備規範文本翻譯如下：
關於OB設備的醫療設備規範文件：
此設備已通過FDA認證，並獲得510(k)許可證。該設備的PMA申請已提交，並在NCT登錄編號為[編號]的研究中進行測試。相關文獻的PMID編號為[編號]。請參考以下識別碼和網址：
識別碼：[識別碼]
網址：[網址]
政策：醫療規範-v1
決定相當於
器材摘要
InTouch Thermal Camera is the device name listed in this FDA 510(k) record. The listed applicant is Intouch Technologies, Inc., D.B.A. Intouch Health. It received FDA 510(k) clearance on 2019-03-25 under 510(k) number K181716. The device is classified under product code LHQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the InTouch Thermal Camera?
InTouch Thermal Camera is a medical device that received FDA 510(k) clearance on 2019-03-25. The listed applicant is Intouch Technologies, Inc., D.B.A. Intouch Health. The 510(k) number is K181716.
When did InTouch Thermal Camera receive FDA 510(k) clearance?
InTouch Thermal Camera received FDA 510(k) clearance on 2019-03-25, under 510(k) number K181716.
Who is the listed applicant for InTouch Thermal Camera?
The FDA 510(k) record lists Intouch Technologies, Inc., D.B.A. Intouch Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InTouch Thermal Camera?
The FDA product code for InTouch Thermal Camera is LHQ.
相關臨床試驗
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相關器械（代碼：LHQ）
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
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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