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)

伊野內氣球A

K 號：K220881 · 2022-12-18

申請人Toray Industries, Inc.
決定日期2022-12-18
產品代碼OZT
諮詢委員會履歷
決定相當於

器材摘要

INOUE BALLOON A is the device name listed in this FDA 510(k) record. The listed applicant is Toray Industries, Inc.. It received FDA 510(k) clearance on 2022-12-18 under 510(k) number K220881. 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 INOUE BALLOON A?

INOUE BALLOON A is a medical device that received FDA 510(k) clearance on 2022-12-18. The listed applicant is Toray Industries, Inc.. The 510(k) number is K220881.

When did INOUE BALLOON A receive FDA 510(k) clearance?

INOUE BALLOON A received FDA 510(k) clearance on 2022-12-18, under 510(k) number K220881.

Who is the listed applicant for INOUE BALLOON A?

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

What is the FDA product code for INOUE BALLOON A?

The FDA product code for INOUE BALLOON A 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。

K253855KardiaPSI 气球心导管Intervention Tech, Inc. ; dba CorventionK260437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.K172932真流閉孔成形灌流心导管C.R. Bard, 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。

↑