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FDA 510(k)

UV燈用於陽光燈產品

K 號:K180581 · 2018-06-22

決定日期2018-06-22
產品代碼LEJ
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

UV Lamps for Sunlamp Products is the device name listed in this FDA 510(k) record. The listed applicant is Feilo Sylvania Germany GmbH. It received FDA 510(k) clearance on 2018-06-22 under 510(k) number K180581. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the UV Lamps for Sunlamp Products?

UV Lamps for Sunlamp Products is a medical device that received FDA 510(k) clearance on 2018-06-22. The listed applicant is Feilo Sylvania Germany GmbH. The 510(k) number is K180581.

When did UV Lamps for Sunlamp Products receive FDA 510(k) clearance?

UV Lamps for Sunlamp Products received FDA 510(k) clearance on 2018-06-22, under 510(k) number K180581.

Who is the listed applicant for UV Lamps for Sunlamp Products?

The FDA 510(k) record lists Feilo Sylvania Germany GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UV Lamps for Sunlamp Products?

The FDA product code for UV Lamps for Sunlamp Products is LEJ.

相關臨床試驗

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相關器械(代碼:LEJ)

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

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