KnoxFog 防霧設備
K 號：K251068 · 2025-08-27
廣告
器材摘要
KnoxFog Anti-fogging Device is the device name listed in this FDA 510(k) record. The listed applicant is Uv One Hygienics, Inc.. It received FDA 510(k) clearance on 2025-08-27 under 510(k) number K251068. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the KnoxFog Anti-fogging Device?
KnoxFog Anti-fogging Device is a medical device that received FDA 510(k) clearance on 2025-08-27. The listed applicant is Uv One Hygienics, Inc.. The 510(k) number is K251068.
When did KnoxFog Anti-fogging Device receive FDA 510(k) clearance?
KnoxFog Anti-fogging Device received FDA 510(k) clearance on 2025-08-27, under 510(k) number K251068.
Who is the listed applicant for KnoxFog Anti-fogging Device?
The FDA 510(k) record lists Uv One Hygienics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KnoxFog Anti-fogging Device?
The FDA product code for KnoxFog Anti-fogging Device is OCT.
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：OCT）
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。
K231822GOLFF 適用於醫療設備之無菌除霧溶液Batrik Medical Manufacturing, Inc.K221293E-Brik 医療設備規範文本
E-Brik 医學視覺輔助設備Jdi Surgical, Inc.K190864康尼克防霧解決方案Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal UrunlerK181887AMD 防霧解決方案Advanced Medical Design Co., Ltd.K163257維特歐防霧溶液Sio2 Nanotech, LLCK152948美林防霧溶液Medline Industries, Inc.
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。
廣告