BTL-899TT
K 號：K252963 · 2026-06-12
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器材摘要
BTL-899TT is the device name listed in this FDA 510(k) record. The listed applicant is BTL Industries, Inc.. It received FDA 510(k) clearance on 2026-06-12 under 510(k) number K252963. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BTL-899TT?
BTL-899TT is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is BTL Industries, Inc.. The 510(k) number is K252963.
When did BTL-899TT receive FDA 510(k) clearance?
BTL-899TT received FDA 510(k) clearance on 2026-06-12, under 510(k) number K252963.
Who is the listed applicant for BTL-899TT?
FDA 510(k) 記錄將 BTL Industries, Inc. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for BTL-899TT?
The FDA product code for BTL-899TT is IMJ.
其他以 BTL Industries, Inc. 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：IMJ）
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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