BTL-754FF
K 號：K252561 · 2026-02-18
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器材摘要
BTL-754FF 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 2026-02-18 under 510(k) number K252561. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常見問題
What is the BTL-754FF?
BTL-754FF is a medical device that received FDA 510(k) clearance on 2026-02-18. The listed applicant is BTL Industries, Inc.. The 510(k) number is K252561.
When did BTL-754FF receive FDA 510(k) clearance?
BTL-754FF received FDA 510(k) clearance on 2026-02-18, under 510(k) number K252561.
Who is the listed applicant for BTL-754FF?
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-754FF?
The FDA product code for BTL-754FF is GEX. This falls under the Gastroenterology category.
其他以 BTL Industries, Inc. 為申請人之記錄
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相關器械（代碼：GEX）
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
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