FDA 510(k)

點尖科學肌酸酐激酶（CK）試劑組

K 號：K191296 · 2020-08-11

決定日期2020-08-11

產品代碼CGS

諮詢委員會CH

決定相當於

器材摘要

Pointe Scientific Creatinine Kinase (CK) Reagent Set is the device name listed in this FDA 510(k) record. The listed applicant is Medtest DX. It received FDA 510(k) clearance on 2020-08-11 under 510(k) number K191296. 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 Pointe Scientific Creatinine Kinase (CK) Reagent Set?

Pointe Scientific Creatinine Kinase (CK) Reagent Set is a medical device that received FDA 510(k) clearance on 2020-08-11. The listed applicant is Medtest DX. The 510(k) number is K191296.

When did Pointe Scientific Creatinine Kinase (CK) Reagent Set receive FDA 510(k) clearance?

Pointe Scientific Creatinine Kinase (CK) Reagent Set received FDA 510(k) clearance on 2020-08-11, under 510(k) number K191296.

Who is the listed applicant for Pointe Scientific Creatinine Kinase (CK) Reagent Set?

The FDA 510(k) record lists Medtest DX as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pointe Scientific Creatinine Kinase (CK) Reagent Set?

The FDA product code for Pointe Scientific Creatinine Kinase (CK) Reagent Set is CGS.

其他以 Medtest DX 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。

K191638點尖科學可卡因代謝物酵素免疫分析

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。

K182702SEKURE 磷酸激酶測試Sekisui Diagnostics P.E.I., Inc.K160724ADVIA 化學肌酸激酶 (CK_L) 檢測，ADVIA 化學酶 3 校正器Siemens Healthcare Diagnostics, Inc.

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。