ANGIO-PRESS LITE DVT 压縮設備
K 號：K173012 · 2018-05-10
廣告
器材摘要
ANGIO-PRESS LITE DVT Compression Device is the device name listed in this FDA 510(k) record. The listed applicant is Pegasus Medical Supply, Inc.. It received FDA 510(k) clearance on 2018-05-10 under 510(k) number K173012. 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 ANGIO-PRESS LITE DVT Compression Device?
ANGIO-PRESS LITE DVT Compression Device is a medical device that received FDA 510(k) clearance on 2018-05-10. The listed applicant is Pegasus Medical Supply, Inc.. The 510(k) number is K173012.
When did ANGIO-PRESS LITE DVT Compression Device receive FDA 510(k) clearance?
ANGIO-PRESS LITE DVT Compression Device received FDA 510(k) clearance on 2018-05-10, under 510(k) number K173012.
Who is the listed applicant for ANGIO-PRESS LITE DVT Compression Device?
The FDA 510(k) record lists Pegasus Medical Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANGIO-PRESS LITE DVT Compression Device?
The FDA product code for ANGIO-PRESS LITE DVT Compression Device is JOW.
相關臨床試驗
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。
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, LLCK253555Flexitouch® Plus 進階氣動壓迫系統Tactile MedicalK253386DVT 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。
廣告