FDA 510(k)

德文恩24R 深部静脈血栓症（DVT）預防治療系統

K 號：K173528 · 2018-02-06

申請人Devon Medical Products (Jiangsu), Ltd.

決定日期2018-02-06

產品代碼JOW

諮詢委員會履歷

決定相當於

器材摘要

Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Devon Medical Products (Jiangsu), Ltd.. It received FDA 510(k) clearance on 2018-02-06 under 510(k) number K173528. 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 Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System?

Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System is a medical device that received FDA 510(k) clearance on 2018-02-06. The listed applicant is Devon Medical Products (Jiangsu), Ltd.. The 510(k) number is K173528.

When did Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System receive FDA 510(k) clearance?

Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System received FDA 510(k) clearance on 2018-02-06, under 510(k) number K173528.

Who is the listed applicant for Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System?

The FDA 510(k) record lists Devon Medical Products (Jiangsu), Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System?

The FDA product code for Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System is JOW.

其他以 Devon Medical Products (Jiangsu), 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。

K190423德文恩24D 深部静脈血栓症（DVT）預防治療系統 K182578德文恩62 深部静脈血栓症（DVT）預防治療設備 K182150德文頓52連續壓縮設備 K172030德文恩51 K170814德文恩24

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。

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官方來源

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