FDA 510(k)Sensilight Pro / 鋒鋒IPL
K 號:K183260 · 2019-03-18
決定日期2019-03-18
產品代碼OHT
諮詢委員會SU
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決定相當於
器材摘要
Sensilight Pro / Pistol IPL is the device name listed in this FDA 510(k) record. The listed applicant is El Global Trade, Ltd.. It received FDA 510(k) clearance on 2019-03-18 under 510(k) number K183260. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Sensilight Pro / Pistol IPL?
Sensilight Pro / Pistol IPL is a medical device that received FDA 510(k) clearance on 2019-03-18. The listed applicant is El Global Trade, Ltd.. The 510(k) number is K183260.
When did Sensilight Pro / Pistol IPL receive FDA 510(k) clearance?
Sensilight Pro / Pistol IPL received FDA 510(k) clearance on 2019-03-18, under 510(k) number K183260.
Who is the listed applicant for Sensilight Pro / Pistol IPL?
The FDA 510(k) record lists El Global Trade, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sensilight Pro / Pistol IPL?
The FDA product code for Sensilight Pro / Pistol IPL is OHT.
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其他以 El Global Trade, Ltd. 為申請人之記錄
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相關器械(代碼:OHT)
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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