FDA 510(k)

Venclose數位RF發生器（VCRFG1）

K 號：K250068 · 2025-02-04

決定日期2025-02-04

產品代碼GEI

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Venclose digiRF Generator (VCRFG1) is the device name listed in this FDA 510(k) record. The listed applicant is Venclose, Inc.. It received FDA 510(k) clearance on 2025-02-04 under 510(k) number K250068. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Venclose digiRF Generator (VCRFG1)?

Venclose digiRF Generator (VCRFG1) is a medical device that received FDA 510(k) clearance on 2025-02-04. The listed applicant is Venclose, Inc.. The 510(k) number is K250068.

When did Venclose digiRF Generator (VCRFG1) receive FDA 510(k) clearance?

Venclose digiRF Generator (VCRFG1) received FDA 510(k) clearance on 2025-02-04, under 510(k) number K250068.

Who is the listed applicant for Venclose digiRF Generator (VCRFG1)?

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

What is the FDA product code for Venclose digiRF Generator (VCRFG1)?

The FDA product code for Venclose digiRF Generator (VCRFG1) is GEI.

其他以 Venclose, 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。

K252316Venclose digiRF 產生器 (VCRFG1)；Venclose EVSRF 穿刺針 (VC10A256F60, VC10A256F100)K211806Venclose digiRF 產生器搭配 Maven 管腔導管，Venclose Maven 系統，Venclose digiRF 產生器，Venclose Maven 管腔導管 K160754Venclose 電波系統（digiRF 產生器，EVSRF 穿刺電極）

相關器械（代碼：GEI）

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。

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官方來源

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