myLEDmask 2 (MJ-144)
K 號：K260415 · 2026-05-12
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器材摘要
myLEDmask 2 (MJ-144) is the device name listed in this FDA 510(k) record. The listed applicant is Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2026-05-12 under 510(k) number K260415. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the myLEDmask 2 (MJ-144)?
myLEDmask 2 (MJ-144) is a medical device that received FDA 510(k) clearance on 2026-05-12. The listed applicant is Light Tree Ventures Europe B.V.. The 510(k) number is K260415.
When did myLEDmask 2 (MJ-144) receive FDA 510(k) clearance?
myLEDmask 2 (MJ-144) received FDA 510(k) clearance on 2026-05-12, under 510(k) number K260415.
Who is the listed applicant for myLEDmask 2 (MJ-144)?
The FDA 510(k) record lists Light Tree Ventures Europe B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for myLEDmask 2 (MJ-144)?
The FDA product code for myLEDmask 2 (MJ-144) is OHS.
相關臨床試驗
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其他以 Light Tree Ventures Europe B.V. 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：OHS）
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
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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