肺Q軟體
K 號：K173821 · 2018-06-05
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器材摘要
LungQ Software is the device name listed in this FDA 510(k) record. The listed applicant is Thirona Corporation. It received FDA 510(k) clearance on 2018-06-05 under 510(k) number K173821. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LungQ Software?
LungQ Software is a medical device that received FDA 510(k) clearance on 2018-06-05. The listed applicant is Thirona Corporation. The 510(k) number is K173821.
When did LungQ Software receive FDA 510(k) clearance?
LungQ Software received FDA 510(k) clearance on 2018-06-05, under 510(k) number K173821.
Who is the listed applicant for LungQ Software?
The FDA 510(k) record lists Thirona Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LungQ Software?
The FDA product code for LungQ Software is JAK.
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相關器械（代碼：JAK）
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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