FDA 510(k)

QXDx BCR-ABL %IS Kit，用於QXDx AutoDG ddPCR系統

K 號：K181661 · 2019-02-13

決定日期2019-02-13

產品代碼OYX

諮詢委員會MG (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories, Inc.. It received FDA 510(k) clearance on 2019-02-13 under 510(k) number K181661. The device is classified under product code OYX. It was reviewed by the MG advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System?

QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System is a medical device that received FDA 510(k) clearance on 2019-02-13. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K181661.

When did QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System receive FDA 510(k) clearance?

QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System received FDA 510(k) clearance on 2019-02-13, under 510(k) number K181661.

Who is the listed applicant for QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System?

The FDA 510(k) record lists Bio-Rad Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System?

The FDA product code for QXDx BCR-ABL %IS Kit for use on the QXDx AutoDG ddPCR System is OYX.

其他以 Bio-Rad Laboratories, 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。

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相關器械（代碼：OYX）

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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