FDA 510(k)

Nuvis®無線高解析度攝影系統（Nuvis-2K）

K 號：K242606 · 2025-11-20

決定日期2025-11-20

產品代碼GCJ

諮詢委員會GU

決定相當於

器材摘要

Nuvis® Wireless HD Camera System (Nuvis-2K) is the device name listed in this FDA 510(k) record. The listed applicant is Integrated Endoscopy, Inc.. It received FDA 510(k) clearance on 2025-11-20 under 510(k) number K242606. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Nuvis® Wireless HD Camera System (Nuvis-2K)?

Nuvis® Wireless HD Camera System (Nuvis-2K) is a medical device that received FDA 510(k) clearance on 2025-11-20. The listed applicant is Integrated Endoscopy, Inc.. The 510(k) number is K242606.

When did Nuvis® Wireless HD Camera System (Nuvis-2K) receive FDA 510(k) clearance?

Nuvis® Wireless HD Camera System (Nuvis-2K) received FDA 510(k) clearance on 2025-11-20, under 510(k) number K242606.

Who is the listed applicant for Nuvis® Wireless HD Camera System (Nuvis-2K)?

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

What is the FDA product code for Nuvis® Wireless HD Camera System (Nuvis-2K)?

The FDA product code for Nuvis® Wireless HD Camera System (Nuvis-2K) is GCJ.

其他以 Integrated Endoscopy, 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。

K191594Nuvis電池內視鏡

相關器械（代碼：GCJ）

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。

K262397CuratOR EX2742Eizo Corporation K260884UNIDRIVE選擇系統Karl Storz SE & CO. KG K260972OEV-271MUH LCD 螢幕；OEV-321MUH LCD 螢幕；OEV-431MUH LCD 螢幕Sony Corporation K261139VereSee (VER150、VER200、VER151、VER201、VER200C 及 VER-100-103)Freyja Healthcare, LLC K253541EZ-Close™（EZ Close Port Site Closing Device、EZ Close MAX Port Site Closing Device、EZ Close II Port Site Closing Device）Medical Impact K261614LED LCD 螢幕 (OEV-271H)Lg Electronics.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。