FDA 510(k)

XR系列（XR-10，XR-20）自動血液學分析儀

K 號：K253212 · 2026-05-27

決定日期2026-05-27

產品代碼GKZ

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

XR-Series (XR-10, XR-20) Automated Hematology Analyzers is the device name listed in this FDA 510(k) record. The listed applicant is Sysmex America, Inc.. It received FDA 510(k) clearance on 2026-05-27 under 510(k) number K253212. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the XR-Series (XR-10, XR-20) Automated Hematology Analyzers?

XR-Series (XR-10, XR-20) Automated Hematology Analyzers is a medical device that received FDA 510(k) clearance on 2026-05-27. The listed applicant is Sysmex America, Inc.. The 510(k) number is K253212.

When did XR-Series (XR-10, XR-20) Automated Hematology Analyzers receive FDA 510(k) clearance?

XR-Series (XR-10, XR-20) Automated Hematology Analyzers received FDA 510(k) clearance on 2026-05-27, under 510(k) number K253212.

Who is the listed applicant for XR-Series (XR-10, XR-20) Automated Hematology Analyzers?

The FDA 510(k) record lists Sysmex America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XR-Series (XR-10, XR-20) Automated Hematology Analyzers?

The FDA product code for XR-Series (XR-10, XR-20) Automated Hematology Analyzers is GKZ.

其他以 Sysmex America, 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。

K250943Sysmex XR系列（XR-10）自動血液學分析儀 K251371Sysmex XR系列（XR-20）自動血液學分析儀 K250965自動血液凝固分析儀CN系列（CN-6000）K230887Sysmex XQ系列（XQ-320）自動血液學分析儀 K210346系統梅克斯 XW-100 自動血液學分析儀 K182389Sysmex XN-L自動血液學分析儀

查看所有 12 項裝置 →

相關器械（代碼：GKZ）

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。

K260781裕米森 H550HORIBA ABX SAS K243348Athelas HomeAthelas, Inc.K251249真血學檢測Truvian Sciences, Inc.K251371Sysmex XR系列（XR-20）自動血液學分析儀Sysmex America, Inc.K250943Sysmex XR系列（XR-10）自動血液學分析儀Sysmex America, Inc.K243283Alinity h-series 系統Abbott Laboratories

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。