ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG校准器, ARCHITECT HSV-2 IgG控制
K 號:K243575 · 2025-02-12
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器材摘要
常見問題
What is the ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls?
ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls is a medical device that received FDA 510(k) clearance on 2025-02-12. The listed applicant is Biokit, S.A.. The 510(k) number is K243575.
When did ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls receive FDA 510(k) clearance?
ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls received FDA 510(k) clearance on 2025-02-12, under 510(k) number K243575.
Who is the listed applicant for ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls?
The FDA 510(k) record lists Biokit, S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls?
The FDA product code for ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls is MYF.
相關臨床試驗
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其他以 Biokit, S.A. 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:MYF)
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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