隧道視野內視鏡軟組織釋放系統及HBL刀片組裝
K 號:K252020 · 2025-10-15
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器材摘要
常見問題
What is the TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly?
TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly is a medical device that received FDA 510(k) clearance on 2025-10-15. The listed applicant is Hand Biomechanics Lab, Inc.. The 510(k) number is K252020.
When did TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly receive FDA 510(k) clearance?
TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly received FDA 510(k) clearance on 2025-10-15, under 510(k) number K252020.
Who is the listed applicant for TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly?
The FDA 510(k) record lists Hand Biomechanics Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly?
The FDA product code for TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly is HRX.
相關臨床試驗
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其他以 Hand Biomechanics Lab, 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:HRX)
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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