免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

Project E Beauty LED 光療面膜(型號:PE730)

K 號:K214101 · 2022-03-23

決定日期2022-03-23
產品代碼OHS
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Project E Beauty LED Light Therapy Mask (Model: PE730) is the device name listed in this FDA 510(k) record. The listed applicant is Duplex International Trading Limited. It received FDA 510(k) clearance on 2022-03-23 under 510(k) number K214101. 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 Project E Beauty LED Light Therapy Mask (Model: PE730)?

Project E Beauty LED Light Therapy Mask (Model: PE730) is a medical device that received FDA 510(k) clearance on 2022-03-23. The listed applicant is Duplex International Trading Limited. The 510(k) number is K214101.

When did Project E Beauty LED Light Therapy Mask (Model: PE730) receive FDA 510(k) clearance?

Project E Beauty LED Light Therapy Mask (Model: PE730) received FDA 510(k) clearance on 2022-03-23, under 510(k) number K214101.

Who is the listed applicant for Project E Beauty LED Light Therapy Mask (Model: PE730)?

FDA 510(k) 記錄將 Duplex International Trading Limited 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Project E Beauty LED Light Therapy Mask (Model: PE730)?

The FDA product code for Project E Beauty LED Light Therapy Mask (Model: PE730) is OHS.

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。

其他以 Duplex International Trading Limited 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。

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。

↑