MR5 活動專業版
K 號：K254024 · 2026-05-19
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器材摘要
MR5 Activ Pro is the device name listed in this FDA 510(k) record. The listed applicant is Multi Radiance Medical, Inc.. It received FDA 510(k) clearance on 2026-05-19 under 510(k) number K254024. The device is classified under product code NHN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MR5 Activ Pro?
MR5 Activ Pro is a medical device that received FDA 510(k) clearance on 2026-05-19. The listed applicant is Multi Radiance Medical, Inc.. The 510(k) number is K254024.
When did MR5 Activ Pro receive FDA 510(k) clearance?
MR5 Activ Pro received FDA 510(k) clearance on 2026-05-19, under 510(k) number K254024.
Who is the listed applicant for MR5 Activ Pro?
The FDA 510(k) record lists Multi Radiance Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MR5 Activ Pro?
The FDA product code for MR5 Activ Pro is NHN.
相關臨床試驗
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相關器械（代碼：NHN）
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。
K251903Erchonia DPN雷射（型號# EVRL）Erchonia CorporationK252273治療美國Dmc Importação E Exportação DE Equipamentos LtdaK241057強化手持式疼痛緩解雷射儀器（GD-P-E）Wuhan Guangdun Technology Co.,Ltd..K232813治療EC，治療XTDmc Importacao E Exportacao DE Equipamentos LtdaK231409Erchonia FX-405Erchonia CorporationK212189維布羅盧克斯Multi Radiance Medical
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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