深CT
K 號：K182875 · 2019-07-10
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器材摘要
DeepCT is the device name listed in this FDA 510(k) record. The listed applicant is Deep01 Limited. It received FDA 510(k) clearance on 2019-07-10 under 510(k) number K182875. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DeepCT?
DeepCT is a medical device that received FDA 510(k) clearance on 2019-07-10. The listed applicant is Deep01 Limited. The 510(k) number is K182875.
When did DeepCT receive FDA 510(k) clearance?
DeepCT received FDA 510(k) clearance on 2019-07-10, under 510(k) number K182875.
Who is the listed applicant for DeepCT?
The FDA 510(k) record lists Deep01 Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DeepCT?
The FDA product code for DeepCT is QAS.
相關臨床試驗
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相關器械（代碼：QAS）
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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