sensiFirm
K 號：K170637 · 2017-07-14
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器材摘要
sensiFirm is the device name listed in this FDA 510(k) record. The listed applicant is El Global Trade, Ltd.. It received FDA 510(k) clearance on 2017-07-14 under 510(k) number K170637. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the sensiFirm?
sensiFirm is a medical device that received FDA 510(k) clearance on 2017-07-14. The listed applicant is El Global Trade, Ltd.. The 510(k) number is K170637.
When did sensiFirm receive FDA 510(k) clearance?
sensiFirm received FDA 510(k) clearance on 2017-07-14, under 510(k) number K170637.
Who is the listed applicant for sensiFirm?
The FDA 510(k) record lists El Global Trade, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for sensiFirm?
The FDA product code for sensiFirm is PBX.
相關臨床試驗
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其他以 El Global Trade, Ltd. 為申請人之記錄
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：PBX）
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。
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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