EUROIMMUN IFA:克氏毛蟻蟻敏感(抗-dsDNA)EUROPattern
K 號:K172252 · 2018-04-20
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器材摘要
常見問題
What is the EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern?
EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern is a medical device that received FDA 510(k) clearance on 2018-04-20. The listed applicant is Euroimmun Us, Inc.. The 510(k) number is K172252.
When did EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern receive FDA 510(k) clearance?
EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern received FDA 510(k) clearance on 2018-04-20, under 510(k) number K172252.
Who is the listed applicant for EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern?
The FDA 510(k) record lists Euroimmun Us, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern?
The FDA product code for EUROIMMUN IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern is KTL.
相關臨床試驗
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其他以 Euroimmun Us, Inc. 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。
相關器械(代碼:KTL)
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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