QSCHECK 医療設備規範文本 QSCHECK 医療設備規範文本
K 號：K252619 · 2026-02-20
廣告
器材摘要
QSCHECK UISACR is the device name listed in this FDA 510(k) record. The listed applicant is Qstag, Inc.. It received FDA 510(k) clearance on 2026-02-20 under 510(k) number K252619. The device is classified under product code JFY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the QSCHECK UISACR?
QSCHECK UISACR is a medical device that received FDA 510(k) clearance on 2026-02-20. The listed applicant is Qstag, Inc.. The 510(k) number is K252619.
When did QSCHECK UISACR receive FDA 510(k) clearance?
QSCHECK UISACR received FDA 510(k) clearance on 2026-02-20, under 510(k) number K252619.
Who is the listed applicant for QSCHECK UISACR?
The FDA 510(k) record lists Qstag, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QSCHECK UISACR?
The FDA product code for QSCHECK UISACR is JFY.
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。
相關器械（代碼：JFY）
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。
K212223Atellica CH 酶促性肌酸酐_3 (ECre3)Siemens Healthcare Diagnostics, Inc.K193649裕米森C1200肌肝酐PAPHORIBA ABX SASK182384ACR LAB 尿液分析測試系統Healthy.Io, Ltd.K183555GEM預警者化學狀態監測系統Instrumentation Laboratory COK182038URiSCAN 10ACR 尿試紙於URiSCAN Optima 尿分析儀上Yd Diagnostics CorporationK182063VITROS化學產品CRBM薄片，VITROS化學產品CREA薄片，VITROS化學產品TBIL薄片，VITROS XT 7600整合系統Ortho-Clinical 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。
廣告