FDA 510(k)

輸血壓力測試器 DVT 型號

K 號：K172277 · 2017-11-03

決定日期2017-11-03

產品代碼JOW

諮詢委員會履歷

決定相當於

器材摘要

Phlebo Press DVT Model is the device name listed in this FDA 510(k) record. The listed applicant is Mego Afek AC , Ltd.. It received FDA 510(k) clearance on 2017-11-03 under 510(k) number K172277. 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 Phlebo Press DVT Model?

Phlebo Press DVT Model is a medical device that received FDA 510(k) clearance on 2017-11-03. The listed applicant is Mego Afek AC , Ltd.. The 510(k) number is K172277.

When did Phlebo Press DVT Model receive FDA 510(k) clearance?

Phlebo Press DVT Model received FDA 510(k) clearance on 2017-11-03, under 510(k) number K172277.

Who is the listed applicant for Phlebo Press DVT Model?

The FDA 510(k) record lists Mego Afek AC , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Phlebo Press DVT Model?

The FDA product code for Phlebo Press DVT Model is JOW.

其他以 Mego Afek AC , Ltd. 為申請人之記錄

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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

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