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)

EPX-4440FN數位視頻處理器，配光源

K 號：K180414 · 2018-05-24

申請人Fujifilm New Development U.S.A., Inc.
決定日期2018-05-24
產品代碼FET
諮詢委員會GU
決定相當於

器材摘要

EPX-4440FN Digital Video Processor with Light Source is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm New Development U.S.A., Inc.. It received FDA 510(k) clearance on 2018-05-24 under 510(k) number K180414. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the EPX-4440FN Digital Video Processor with Light Source?

EPX-4440FN Digital Video Processor with Light Source is a medical device that received FDA 510(k) clearance on 2018-05-24. The listed applicant is Fujifilm New Development U.S.A., Inc.. The 510(k) number is K180414.

When did EPX-4440FN Digital Video Processor with Light Source receive FDA 510(k) clearance?

EPX-4440FN Digital Video Processor with Light Source received FDA 510(k) clearance on 2018-05-24, under 510(k) number K180414.

Who is the listed applicant for EPX-4440FN Digital Video Processor with Light Source?

The FDA 510(k) record lists Fujifilm New Development U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPX-4440FN Digital Video Processor with Light Source?

The FDA product code for EPX-4440FN Digital Video Processor with Light Source is FET.

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 Fujifilm New Development U.S.A., 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。

K162836富士菲林外科系統K170084互鎖針鞘

相關器械（代碼：FET）

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。

K2620794K攝影鏡頭 OLYMPUS CH-S700-08-LB 医療設備規範文本Olympus Medical Systems Corp.K261880富士通電子處理器EP-8000；氣球控制器PB-30；內視鏡輔助程序EW10-VM01Fujifilm CorporationK261260HD攝影鏡頭 OLYMPUS CH-S200-08-LBOlympus Medical Systems CorporationK251734ProVee影片處理單元（PV-003）Proverum LimitedK250462UL UHD-Clear View 4K攝影系統（UL-3Chip 4K）Univlabs Technologies Private LimitedK250204內視鏡攝影系統Shenzhen Sophway Technology Co., Ltd.

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。

↑