FDA 510(k)

德文恩24

K 號：K170814 · 2017-07-11

申請人Devon Medical Products (Jiangsu), Ltd.

決定日期2017-07-11

產品代碼JOW

諮詢委員會履歷

決定相當於

器材摘要

Devon 24 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 2017-07-11 under 510(k) number K170814. 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 24?

Devon 24 is a medical device that received FDA 510(k) clearance on 2017-07-11. The listed applicant is Devon Medical Products (Jiangsu), Ltd.. The 510(k) number is K170814.

When did Devon 24 receive FDA 510(k) clearance?

Devon 24 received FDA 510(k) clearance on 2017-07-11, under 510(k) number K170814.

Who is the listed applicant for Devon 24?

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 24?

The FDA product code for Devon 24 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 K173528德文恩24R 深部静脈血栓症（DVT）預防治療系統 K172030德文恩51

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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