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K 號:K241571 · 2024-08-14
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器材摘要
常見問題
What is the BostonSight® Specialty Lenses?
BostonSight® Specialty Lenses is a medical device that received FDA 510(k) clearance on 2024-08-14. The listed applicant is Boston Foundation For Sight, Inc. D/B/A Bostonsight. The 510(k) number is K241571.
When did BostonSight® Specialty Lenses receive FDA 510(k) clearance?
BostonSight® Specialty Lenses received FDA 510(k) clearance on 2024-08-14, under 510(k) number K241571.
Who is the listed applicant for BostonSight® Specialty Lenses?
The FDA 510(k) record lists Boston Foundation For Sight, Inc. D/B/A Bostonsight as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BostonSight® Specialty Lenses?
The FDA product code for BostonSight® Specialty Lenses is HQD.
相關臨床試驗
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:HQD)
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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