免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料，僅供一般參考，不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

MEDRAD Stellant FLEX CT 注射系統搭配 Certegra 工作站，MEDRAD Stellant FLEX 静脈注射套件，MEDRAD Stellant CT 注射系統搭配 Certegra 工作站，MEDRAD Stellant 静脈注射套件，MEDRAD Stellant 接頭管路，P3T 心臟，P3T 肺動脈，P3T 腹部，ISI，Connect.CT

K 號：K182273 · 2018-11-01

申請人Bayer Medical Care, Inc.
決定日期2018-11-01
產品代碼DXT
諮詢委員會履歷
決定相當於

器材摘要

MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT is the device name listed in this FDA 510(k) record. The listed applicant is Bayer Medical Care, Inc.. It received FDA 510(k) clearance on 2018-11-01 under 510(k) number K182273. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT?

MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT is a medical device that received FDA 510(k) clearance on 2018-11-01. The listed applicant is Bayer Medical Care, Inc.. The 510(k) number is K182273.

When did MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT receive FDA 510(k) clearance?

MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT received FDA 510(k) clearance on 2018-11-01, under 510(k) number K182273.

Who is the listed applicant for MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT?

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

What is the FDA product code for MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT?

The FDA product code for MEDRAD Stellant FLEX CT Injection System with Certegra Workstation, MEDRAD Stellant FLEX Syringe Kits, MEDRAD Stellant CT Injection System with Certegra Workstation, MEDRAD Stellant Syringe Kits, MEDRAD Stellant Connector Tubing, P3T Cardiac, P3T PA, P3T Abdomen, ISI, Connect.CT is DXT.

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

其他以 Bayer Medical Care, 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。

K253688MEDRAD® 影像大量包裝轉移針K252891MEDRAD MRXperion MR注射系統及MR注射系統針筒組；MEDRAD ISI2 模組（ISI2）K250893球節導向陣列（66295）K200280醫療設備規範文本翻譯： MEDRAD影像大量包裝轉移針K192370MEDRAD Stellant FLEX CT 注射系統搭配 Certegra 工作站K193028MEDRAD 馬克7 頸動脈注射系統

查看所有 9 項裝置 →

相關器械（代碼：DXT）

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。

K252652用於高壓注射器之拋棄式注射器及配件 (900103T); 用於高壓注射器之拋棄式注射器及配件 (900103H); 用於高壓注射器之拋棄式注射器及配件 (801800H); 用於高壓注射器之拋棄式注射器及配件 (800099T); 用於高壓注射器之拋棄式注射器及配件 (800099H); 用於高壓注射器之拋棄式注射器及配件 (800096T); 用於高壓注射器之拋棄式注射器及配件 (800096H); 拋棄式注射器Fortis Biosolutions Company LimitedK252638VeraPro S100 多用針筒 (018808)；VeraPro S100 LV1 低濃度單次使用針筒 (018811)；VeraPro AMT 自動分配器和傳感器 (018814)；VeraPro AngioTouch FLX165 手控器套件 (018806)；VeraPro AngioTouch HiFi165 手控器套件 (018804)Acist Medical Systems, Inc.K252653ACIST Pro 诊断系統 (019304)；處理單元床架；AngioTouch 模組；ACIST Pro 車；單晶體傳感器電纜；三晶體傳感器電纜Acist Medical Systems, Inc.K253048高壓針筒；壓力連接管；快速填充管；針頭；轉移管Shenzhen Maiwei Biotech Co., Ltd.K251788延伸管Zhuhai DR Medical Instruments Co., Ltd.K252891MEDRAD MRXperion MR注射系統及MR注射系統針筒組；MEDRAD ISI2 模組（ISI2）Bayer Medical Care, 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。

↑