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FDA 510(k)

VeraPro 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)

K 號：K252638 · 2026-05-13

申請人Acist Medical Systems, Inc.
決定日期2026-05-13
產品代碼DXT
諮詢委員會履歷
決定相當於

器材摘要

VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804) is the device name listed in this FDA 510(k) record. The listed applicant is Acist Medical Systems, Inc.. It received FDA 510(k) clearance on 2026-05-13 under 510(k) number K252638. 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 VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804)?

VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804) is a medical device that received FDA 510(k) clearance on 2026-05-13. The listed applicant is Acist Medical Systems, Inc.. The 510(k) number is K252638.

When did VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804) receive FDA 510(k) clearance?

VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804) received FDA 510(k) clearance on 2026-05-13, under 510(k) number K252638.

Who is the listed applicant for VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804)?

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

What is the FDA product code for VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804)?

The FDA product code for VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804) 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 Acist Medical Systems, 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。

K262115VueJect® 超聲波增強劑輸送系統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K233904ACIST RXi 系統 (016616)；ACIST Navvus II 針 (016675_)K203004ACIST CVi1 對比劑輸送系統，ACIST CVi 對比劑輸送系統K193183ACIST HDi 系統，ACIST Kodama 靜脈內超聲波針K190473ACIST RXi 系統和 Navvus II 針

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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 LimitedK252653ACIST 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.K244038高壓管路Shandong Int Medical Instruments Co., Ltd.

官方來源

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