痤瘡光療棒
K 號：K160691 · 2016-06-21
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器材摘要
Acne Light Therapy Wand is the device name listed in this FDA 510(k) record. The listed applicant is Zuko, Inc.. It received FDA 510(k) clearance on 2016-06-21 under 510(k) number K160691. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Acne Light Therapy Wand?
Acne Light Therapy Wand is a medical device that received FDA 510(k) clearance on 2016-06-21. The listed applicant is Zuko, Inc.. The 510(k) number is K160691.
When did Acne Light Therapy Wand receive FDA 510(k) clearance?
Acne Light Therapy Wand received FDA 510(k) clearance on 2016-06-21, under 510(k) number K160691.
Who is the listed applicant for Acne Light Therapy Wand?
The FDA 510(k) record lists Zuko, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Acne Light Therapy Wand?
The FDA product code for Acne Light Therapy Wand is OLP.
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：OLP）
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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