再生EMS椅子
K 號：K251026 · 2025-08-29
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器材摘要
Regenesis EMS Chair is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Medical Solutions. It received FDA 510(k) clearance on 2025-08-29 under 510(k) number K251026. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Regenesis EMS Chair?
Regenesis EMS Chair is a medical device that received FDA 510(k) clearance on 2025-08-29. The listed applicant is Trinity Medical Solutions. The 510(k) number is K251026.
When did Regenesis EMS Chair receive FDA 510(k) clearance?
Regenesis EMS Chair received FDA 510(k) clearance on 2025-08-29, under 510(k) number K251026.
Who is the listed applicant for Regenesis EMS Chair?
The FDA 510(k) record lists Trinity Medical Solutions as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Regenesis EMS Chair?
The FDA product code for Regenesis EMS Chair is KPI.
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：KPI）
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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