FDA 510(k)

VITROS BRAHMS PCT試劑包及校准器

K 號：K200236 · 2020-02-25

決定日期2020-02-25

產品代碼PMT

諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)

決定相當於

器材摘要

VITROS BRAHMS PCT Reagent Pack and Calibrators is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Clinical Diagnostics. It received FDA 510(k) clearance on 2020-02-25 under 510(k) number K200236. The device is classified under product code PMT. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the VITROS BRAHMS PCT Reagent Pack and Calibrators?

VITROS BRAHMS PCT Reagent Pack and Calibrators is a medical device that received FDA 510(k) clearance on 2020-02-25. The listed applicant is Ortho Clinical Diagnostics. The 510(k) number is K200236.

When did VITROS BRAHMS PCT Reagent Pack and Calibrators receive FDA 510(k) clearance?

VITROS BRAHMS PCT Reagent Pack and Calibrators received FDA 510(k) clearance on 2020-02-25, under 510(k) number K200236.

Who is the listed applicant for VITROS BRAHMS PCT Reagent Pack and Calibrators?

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

What is the FDA product code for VITROS BRAHMS PCT Reagent Pack and Calibrators?

The FDA product code for VITROS BRAHMS PCT Reagent Pack and Calibrators is PMT.

其他以 Ortho Clinical Diagnostics 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：PMT）

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。

K181002Atellica IM BRAHMS Procalcitonin (PCT)Siemens Healthcare Diagnostics, Inc.K160911VIDAS B.R.A.H.M.S. PCT (PCT)bioMerieux, Inc.K160729電鋒 BRAHMS PCT，電鋒 BRAHMS PCT CalCheck 5Roche Diagnostics

官方來源

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