FDA 510(k)

ADVIA 化學肌酸激酶 (CK_L) 檢測，ADVIA 化學酶 3 校正器

K 號：K160724 · 2016-09-07

決定日期2016-09-07

產品代碼CGS

諮詢委員會CH

決定相當於

器材摘要

ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare Diagnostics, Inc.. It received FDA 510(k) clearance on 2016-09-07 under 510(k) number K160724. The device is classified under product code CGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator?

ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator is a medical device that received FDA 510(k) clearance on 2016-09-07. The listed applicant is Siemens Healthcare Diagnostics, Inc.. The 510(k) number is K160724.

When did ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator receive FDA 510(k) clearance?

ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator received FDA 510(k) clearance on 2016-09-07, under 510(k) number K160724.

Who is the listed applicant for ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator?

FDA 510(k) 記錄將西门子醫療診斷公司列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator?

The FDA product code for ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator is CGS.

其他以 Siemens Healthcare Diagnostics, Inc. 為申請人之記錄

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相關器械（代碼：CGS）

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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官方來源

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