MedHealth DVT壓縮設備 MHH900S/MHH900E
K 號：K231801 · 2023-12-14
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器材摘要
MedHealth DVT compression Devices MHH900S/MHH900E is the device name listed in this FDA 510(k) record. The listed applicant is Medhealth Medical Limited. It received FDA 510(k) clearance on 2023-12-14 under 510(k) number K231801. 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 MedHealth DVT compression Devices MHH900S/MHH900E?
MedHealth DVT compression Devices MHH900S/MHH900E is a medical device that received FDA 510(k) clearance on 2023-12-14. The listed applicant is Medhealth Medical Limited. The 510(k) number is K231801.
When did MedHealth DVT compression Devices MHH900S/MHH900E receive FDA 510(k) clearance?
MedHealth DVT compression Devices MHH900S/MHH900E received FDA 510(k) clearance on 2023-12-14, under 510(k) number K231801.
Who is the listed applicant for MedHealth DVT compression Devices MHH900S/MHH900E?
The FDA 510(k) record lists Medhealth Medical Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E?
The FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E is JOW.
相關臨床試驗
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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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