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FDA 510(k)

KardiaPSI 气球心导管

K 號：K253855 · 2026-05-06

申請人Intervention Tech, Inc. ; dba Corvention
決定日期2026-05-06
產品代碼OZT
諮詢委員會履歷
決定相當於

器材摘要

KardiaPSI Balloon Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Intervention Tech, Inc. ; dba Corvention. It received FDA 510(k) clearance on 2026-05-06 under 510(k) number K253855. The device is classified under product code OZT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the KardiaPSI Balloon Catheter?

KardiaPSI Balloon Catheter is a medical device that received FDA 510(k) clearance on 2026-05-06. The listed applicant is Intervention Tech, Inc. ; dba Corvention. The 510(k) number is K253855.

When did KardiaPSI Balloon Catheter receive FDA 510(k) clearance?

KardiaPSI Balloon Catheter received FDA 510(k) clearance on 2026-05-06, under 510(k) number K253855.

Who is the listed applicant for KardiaPSI Balloon Catheter?

The FDA 510(k) record lists Intervention Tech, Inc. ; dba Corvention as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KardiaPSI Balloon Catheter?

The FDA product code for KardiaPSI Balloon Catheter is OZT.

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

相關器械（代碼：OZT）

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。

K260437心瓣膜成形氣球导管（ValvuloPro）Dongguan TT Medical, Inc.K241562OutFlo 鳩膝瓣擴張氣球針管Disa MedinotecK240967ValvuloPro 門腔擴張氣球針管Dongguan TT Medical, Inc.K231814ValvuloPro 門腔擴張氣球針管Dongguan TT Medical, Inc.K220881伊野內氣球AToray Industries, Inc.K172932真流閉孔成形灌流心导管C.R. Bard, Inc.

官方來源

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