DVT運動氣壓裝置
K 號：K232270 · 2024-03-06
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器材摘要
DVT Motion Pneumatic Compression Device is the device name listed in this FDA 510(k) record. The listed applicant is Koge Micro Tech Co., Ltd.. It received FDA 510(k) clearance on 2024-03-06 under 510(k) number K232270. 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 DVT Motion Pneumatic Compression Device?
DVT Motion Pneumatic Compression Device is a medical device that received FDA 510(k) clearance on 2024-03-06. The listed applicant is Koge Micro Tech Co., Ltd.. The 510(k) number is K232270.
When did DVT Motion Pneumatic Compression Device receive FDA 510(k) clearance?
DVT Motion Pneumatic Compression Device received FDA 510(k) clearance on 2024-03-06, under 510(k) number K232270.
Who is the listed applicant for DVT Motion Pneumatic Compression Device?
The FDA 510(k) record lists Koge Micro Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DVT Motion Pneumatic Compression Device?
The FDA product code for DVT Motion Pneumatic 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。
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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。
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