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FDA 510(k)

CP3000 凝血分析儀，Coagpia AT 製劑，Coagpia 校正儀，Coagpia 控制組合

K 號：K173202 · 2018-05-09

申請人Sekisui Medical Co., Ltd.
決定日期2018-05-09
產品代碼JPA
諮詢委員會HE 請提供完整的描述文本，以便我能夠進行翻譯。
決定相當於

器材摘要

CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set is the device name listed in this FDA 510(k) record. The listed applicant is Sekisui Medical Co., Ltd.. It received FDA 510(k) clearance on 2018-05-09 under 510(k) number K173202. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set?

CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set is a medical device that received FDA 510(k) clearance on 2018-05-09. The listed applicant is Sekisui Medical Co., Ltd.. The 510(k) number is K173202.

When did CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set receive FDA 510(k) clearance?

CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set received FDA 510(k) clearance on 2018-05-09, under 510(k) number K173202.

Who is the listed applicant for CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set?

The FDA 510(k) record lists Sekisui Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set?

The FDA product code for CP3000 Coagulation analyzer, Coagpia AT Reagent, Coagpia Calibrator, Coagpia Control Set is JPA.

相關臨床試驗

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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