UA-細胞完整版
K 號：K170091 · 2017-02-09
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器材摘要
UA-Cellular Complete is the device name listed in this FDA 510(k) record. The listed applicant is Streck. It received FDA 510(k) clearance on 2017-02-09 under 510(k) number K170091. The device is classified under product code JJW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the UA-Cellular Complete?
UA-Cellular Complete is a medical device that received FDA 510(k) clearance on 2017-02-09. The listed applicant is Streck. The 510(k) number is K170091.
When did UA-Cellular Complete receive FDA 510(k) clearance?
UA-Cellular Complete received FDA 510(k) clearance on 2017-02-09, under 510(k) number K170091.
Who is the listed applicant for UA-Cellular Complete?
The FDA 510(k) record lists Streck as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UA-Cellular Complete?
The FDA product code for UA-Cellular Complete is JJW.
相關臨床試驗
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其他以 Streck 為申請人之記錄
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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