FDA 510(k)

Venera 608 深部静脈血栓（DVT）預防系統

K 號：K241096 · 2025-01-15

申請人Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

決定日期2025-01-15

產品代碼JOW

諮詢委員會履歷

決定相當於

器材摘要

Venera 608 Deep Vein Thrombosis (DVT) Prevention System is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. It received FDA 510(k) clearance on 2025-01-15 under 510(k) number K241096. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

Venera 608 Deep Vein Thrombosis (DVT) Prevention System is a medical device that received FDA 510(k) clearance on 2025-01-15. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K241096.

When did Venera 608 Deep Vein Thrombosis (DVT) Prevention System receive FDA 510(k) clearance?

Venera 608 Deep Vein Thrombosis (DVT) Prevention System received FDA 510(k) clearance on 2025-01-15, under 510(k) number K241096.

Who is the listed applicant for Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

The FDA 510(k) record lists Suzhou Minhua Medical Apparatus Supplies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Venera 608 Deep Vein Thrombosis (DVT) Prevention System?

The FDA product code for Venera 608 Deep Vein Thrombosis (DVT) Prevention System is JOW.

其他以 Suzhou Minhua Medical Apparatus Supplies Co., Ltd. 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。

K233276可重用血壓袖帶 K180389維納拉508深部静脈血栓形成（DVT）預防系統 K171889可重用血壓袖帶

相關器械（代碼：JOW）

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。

K261807連續循環器（SC-4004-DL，SC-4008-DL）Bio Compression Systems, Inc.K254217AerloomEvolym, LLC K253555Flexitouch® Plus 進階氣動壓迫系統Tactile Medical K253386DVT 裝備Vistar Medical Supplies Co., Ltd.K250242壓力治療設備（LGT-2202DVT）Guangzhou Longest Medical Technology Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , 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。