VesoFlow Lite 靜脈血栓形成壓力輔助設備
K 號：K181217 · 2018-08-05
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器材摘要
VesoFlow Lite DVT Compression Device is the device name listed in this FDA 510(k) record. The listed applicant is Caremed Supply, Inc.. It received FDA 510(k) clearance on 2018-08-05 under 510(k) number K181217. 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 VesoFlow Lite DVT Compression Device?
VesoFlow Lite DVT Compression Device is a medical device that received FDA 510(k) clearance on 2018-08-05. The listed applicant is Caremed Supply, Inc.. The 510(k) number is K181217.
When did VesoFlow Lite DVT Compression Device receive FDA 510(k) clearance?
VesoFlow Lite DVT Compression Device received FDA 510(k) clearance on 2018-08-05, under 510(k) number K181217.
Who is the listed applicant for VesoFlow Lite DVT Compression Device?
The FDA 510(k) record lists Caremed Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VesoFlow Lite DVT Compression Device?
The FDA product code for VesoFlow Lite DVT Compression Device is JOW.
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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, 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
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